11-47306664-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306664
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306664
    reference: chr 11
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2330A>G
  hgvsp: ENSP00000343902.4:p.Tyr777Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+48A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2330A>G
  hgvsp: ENSP00000304505.6:p.Tyr777Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2330A>G
  hgvsp: ENSP00000310933.4:p.Tyr777Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2330A>G
  hgvsp: ENSP00000378745.3:p.Tyr777Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+48A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+48A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+48A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2330A>G
  hgvsp: ENSP00000384287.2:p.Tyr777Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+48A>G
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Tyr777Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

11-47306667-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306667
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306667
    reference: chr 11
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2333G>A
  hgvsp: ENSP00000304505.6:p.Gly778Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2333G>A
  hgvsp: ENSP00000384287.2:p.Gly778Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+51G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+51G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2333G>A
  hgvsp: ENSP00000378745.3:p.Gly778Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2333G>A
  hgvsp: ENSP00000343902.4:p.Gly778Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2333G>A
  hgvsp: ENSP00000310933.4:p.Gly778Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+51G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+51G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+51G>A
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25197
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly778Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

11-47306673-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306673
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306673
    reference: chr 11
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+57C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2339C>T
  hgvsp: ENSP00000310933.4:p.Pro780Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+57C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2339C>T
  hgvsp: ENSP00000343902.4:p.Pro780Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2339C>T
  hgvsp: ENSP00000384287.2:p.Pro780Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+57C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2339C>T
  hgvsp: ENSP00000304505.6:p.Pro780Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2339C>T
  hgvsp: ENSP00000378745.3:p.Pro780Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+57C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+57C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25203
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro780Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

11-47306677-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306677
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306678
    reference: chr 11
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+62dupG
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+62dupG
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2344dupG
  hgvsp: ENSP00000304505.6:p.Glu782GlyfsTer4
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2344dupG
  hgvsp: ENSP00000343902.4:p.Glu782GlyfsTer4
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+62dupG
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+62dupG
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2344dupG
  hgvsp: ENSP00000310933.4:p.Glu782GlyfsTer4
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2344dupG
  hgvsp: ENSP00000378745.3:p.Glu782GlyfsTer4
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+62dupG
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2344dupG
  hgvsp: ENSP00000384287.2:p.Glu782GlyfsTer4
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu782GlyfsTer4
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

11-47306680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306680
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306680
    reference: chr 11
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2346G>A
  hgvsp: ENST00000349238.3:c.2346G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+64G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+64G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2346G>A
  hgvsp: ENST00000402192.2:c.2346G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2346G>A
  hgvsp: ENST00000342922.4:c.2346G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+64G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+64G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2346G>A
  hgvsp: ENST00000311027.5:c.2346G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+64G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2346G>A
  hgvsp: ENST00000395336.3:c.2346G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13752
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25216
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu782Glu
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-47306684-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306684
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306684
    reference: chr 11
allele count: 7
allele frequency: 5.772814989526464e-5
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+68G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2350G>A
  hgvsp: ENSP00000384287.2:p.Asp784Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+68G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2350G>A
  hgvsp: ENSP00000304505.6:p.Asp784Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+68G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+68G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2350G>A
  hgvsp: ENSP00000310933.4:p.Asp784Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2350G>A
  hgvsp: ENSP00000343902.4:p.Asp784Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+68G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2350G>A
  hgvsp: ENSP00000378745.3:p.Asp784Asn
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13748
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25191
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp784Asn
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-47306686-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306686
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306686
    reference: chr 11
allele count: 1
allele frequency: 8.247286642694553e-6
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2352T>A
  hgvsp: ENSP00000304505.6:p.Asp784Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2352T>A
  hgvsp: ENSP00000310933.4:p.Asp784Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+70T>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+70T>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2352T>A
  hgvsp: ENSP00000343902.4:p.Asp784Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+70T>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2352T>A
  hgvsp: ENSP00000384287.2:p.Asp784Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+70T>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2352T>A
  hgvsp: ENSP00000378745.3:p.Asp784Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+70T>A
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13747
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp784Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-47306696-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306696
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306696
    reference: chr 11
allele count: 2
allele frequency: 1.650437365901964e-5
allele num: 121180
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2362C>G
  hgvsp: ENSP00000310933.4:p.Gln788Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+80C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+80C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+80C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2362C>G
  hgvsp: ENSP00000384287.2:p.Gln788Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+80C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2362C>G
  hgvsp: ENSP00000304505.6:p.Gln788Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+80C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2362C>G
  hgvsp: ENSP00000378745.3:p.Gln788Glu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2362C>G
  hgvsp: ENSP00000343902.4:p.Gln788Glu
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3915
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln788Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-47306705-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306705
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306705
    reference: chr 11
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2371A>C
  hgvsp: ENSP00000378745.3:p.Ser791Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+89A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+89A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2371A>C
  hgvsp: ENSP00000343902.4:p.Ser791Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+89A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2371A>C
  hgvsp: ENSP00000304505.6:p.Ser791Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+89A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2371A>C
  hgvsp: ENSP00000384287.2:p.Ser791Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2371A>C
  hgvsp: ENSP00000310933.4:p.Ser791Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+89A>C
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser791Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

11-47306705-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306705
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306705
    reference: chr 11
allele count: 5
allele frequency: 4.128955539406752e-5
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2371A>G
  hgvsp: ENSP00000310933.4:p.Ser791Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+89A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+89A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+89A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2371A>G
  hgvsp: ENSP00000384287.2:p.Ser791Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2371A>G
  hgvsp: ENSP00000304505.6:p.Ser791Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2371A>G
  hgvsp: ENSP00000343902.4:p.Ser791Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+89A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2371A>G
  hgvsp: ENSP00000378745.3:p.Ser791Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+89A>G
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser791Gly
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD

11-47306705-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306705
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306705
    reference: chr 11
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+89A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2371A>T
  hgvsp: ENSP00000310933.4:p.Ser791Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2371A>T
  hgvsp: ENSP00000343902.4:p.Ser791Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+89A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+89A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2371A>T
  hgvsp: ENSP00000304505.6:p.Ser791Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+89A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+89A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2371A>T
  hgvsp: ENSP00000384287.2:p.Ser791Cys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2371A>T
  hgvsp: ENSP00000378745.3:p.Ser791Cys
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser791Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-47306706-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306706
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306706
    reference: chr 11
allele count: 1
allele frequency: 8.258729477057249e-6
allele num: 121084
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+90G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+90G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2372G>A
  hgvsp: ENSP00000304505.6:p.Ser791Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2372G>A
  hgvsp: ENSP00000310933.4:p.Ser791Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+90G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2372G>A
  hgvsp: ENSP00000384287.2:p.Ser791Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+90G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2372G>A
  hgvsp: ENSP00000343902.4:p.Ser791Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2372G>A
  hgvsp: ENSP00000378745.3:p.Ser791Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+90G>A
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1667
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser791Asn
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-47306708-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306708
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306709
    reference: chr 11
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+93dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2375dupA
  hgvsp: ENSP00000378745.3:p.Tyr792Ter
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+93dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2375dupA
  hgvsp: ENSP00000384287.2:p.Tyr792Ter
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2375dupA
  hgvsp: ENSP00000304505.6:p.Tyr792Ter
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2375dupA
  hgvsp: ENSP00000310933.4:p.Tyr792Ter
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+93dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+93dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+93dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2375dupA
  hgvsp: ENSP00000343902.4:p.Tyr792Ter
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24962
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr792Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

11-47306718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306718
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306718
    reference: chr 11
allele count: 1
allele frequency: 8.271845945141119e-6
allele num: 120892
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2384G>A
  hgvsp: ENSP00000310933.4:p.Arg795Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2384G>A
  hgvsp: ENSP00000304505.6:p.Arg795Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2384G>A
  hgvsp: ENSP00000378745.3:p.Arg795Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+102G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2384G>A
  hgvsp: ENSP00000384287.2:p.Arg795Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+102G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+102G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+102G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2384G>A
  hgvsp: ENSP00000343902.4:p.Arg795Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+102G>A
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg795Gln
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

11-47306724-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306724
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306724
    reference: chr 11
allele count: 1
allele frequency: 8.278145695364238e-6
allele num: 120800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+108G>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2390G>C
  hgvsp: ENSP00000310933.4:p.Ser797Thr
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2390G>C
  hgvsp: ENSP00000343902.4:p.Ser797Thr
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+108G>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2390G>C
  hgvsp: ENSP00000378745.3:p.Ser797Thr
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2390G>C
  hgvsp: ENSP00000384287.2:p.Ser797Thr
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2390G>C
  hgvsp: ENSP00000304505.6:p.Ser797Thr
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+108G>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+108G>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+108G>C
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30032
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser797Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

11-47306742-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306742
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306742
    reference: chr 11
allele count: 9
allele frequency: 7.504377553572918e-5
allele num: 119930
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2408A>G
  hgvsp: ENSP00000384287.2:p.Asn803Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+126A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+126A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2408A>G
  hgvsp: ENSP00000304505.6:p.Asn803Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+126A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+126A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+126A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2408A>G
  hgvsp: ENSP00000310933.4:p.Asn803Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2408A>G
  hgvsp: ENSP00000343902.4:p.Asn803Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2408A>G
  hgvsp: ENSP00000378745.3:p.Asn803Ser
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23219
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn803Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-47306744-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306744
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306744
    reference: chr 11
allele count: 2
allele frequency: 1.67022982362373e-5
allele num: 119744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2410C>T
  hgvsp: ENSP00000304505.6:p.Arg804Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+128C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2410C>T
  hgvsp: ENSP00000384287.2:p.Arg804Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+128C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2410C>T
  hgvsp: ENSP00000378745.3:p.Arg804Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+128C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2410C>T
  hgvsp: ENSP00000310933.4:p.Arg804Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2410C>T
  hgvsp: ENSP00000343902.4:p.Arg804Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+128C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+128C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10571
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22819
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg804Trp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-47306745-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306745
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306745
    reference: chr 11
allele count: 3
allele frequency: 2.505930702662969e-5
allele num: 119716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+129G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411G>A
  hgvsp: ENSP00000384287.2:p.Arg804Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+129G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411G>A
  hgvsp: ENSP00000378745.3:p.Arg804Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411G>A
  hgvsp: ENSP00000304505.6:p.Arg804Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+129G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411G>A
  hgvsp: ENSP00000343902.4:p.Arg804Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+129G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411G>A
  hgvsp: ENSP00000310933.4:p.Arg804Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+129G>A
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg804Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP

11-47306745-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306745
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306745
    reference: chr 11
allele count: 2
allele frequency: 1.670620468441979e-5
allele num: 119716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411G>T
  hgvsp: ENSP00000304505.6:p.Arg804Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+129G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+129G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+129G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411G>T
  hgvsp: ENSP00000384287.2:p.Arg804Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+129G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411G>T
  hgvsp: ENSP00000343902.4:p.Arg804Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411G>T
  hgvsp: ENSP00000378745.3:p.Arg804Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+129G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411G>T
  hgvsp: ENSP00000310933.4:p.Arg804Leu
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11844
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10762
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg804Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-47306756-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306756
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306756
    reference: chr 11
allele count: 1
allele frequency: 8.40180806909647e-6
allele num: 119022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+11G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+140G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+11G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+11G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+140G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+140G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+11G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+11G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+140G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+140G>A
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8007
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26147
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

11-47306759-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306759
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306759
    reference: chr 11
allele count: 1
allele frequency: 8.417650128790047e-6
allele num: 118798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+143C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+14C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+143C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+14C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+143C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+143C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+143C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+14C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+14C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+14C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10681
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1645
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-47306762-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306762
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306762
    reference: chr 11
allele count: 3
allele frequency: 2.527379949452401e-5
allele num: 118700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+146C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+17C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+146C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+146C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+17C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+17C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+17C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+146C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+146C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+17C>A
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10512
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7721
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

11-47306764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306764
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306764
    reference: chr 11
allele count: 8
allele frequency: 6.747069241798093e-5
allele num: 118570
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+148C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+19C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+19C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+19C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+148C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+148C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+148C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+19C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+148C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+19C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19352
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10619
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10385
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2454
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7618
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-47306767-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306767
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306767
    reference: chr 11
allele count: 1
allele frequency: 8.442665856170744e-6
allele num: 118446
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+22C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+151C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+22C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+22C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+151C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+151C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+22C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+151C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+151C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+22C>G
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23146
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

11-47306775-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306775
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306775
    reference: chr 11
allele count: 1
allele frequency: 8.468691248454463e-6
allele num: 118082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+30G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+159G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+159G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+30G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+159G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+159G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+159G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+30G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+30G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+30G>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2427
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4163
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

11-47306788-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306788
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306788
    reference: chr 11
allele count: 2
allele frequency: 1.708146148984507e-5
allele num: 117086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+172C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+43C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+172C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+172C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+172C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+43C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+43C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+43C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+172C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+43C>G
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9281
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13867
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

11-47306789-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306789
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306789
    reference: chr 11
allele count: 3
allele frequency: 2.56213169356905e-5
allele num: 117090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+44T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+173T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+173T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+44T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+44T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+44T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+173T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+173T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+173T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+44T>C
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9240
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14582
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS

11-47306790-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306790
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306790
    reference: chr 11
allele count: 1
allele frequency: 8.557247989046722e-6
allele num: 116860
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2411+45C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2411+45C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.120+174C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2411+45C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2411+45C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2282+174C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2411+45C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2282+174C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2282+174C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2282+174C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8835
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11288
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3637
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2744
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

11-47306952-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306952
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306952
    reference: chr 11
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2283-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2283-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2412-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2412-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2283-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.121-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.131A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2412-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2412-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2283-50A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2412-50A>T
  variant of: http://identifiers.org/hgnc/6766
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14733
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD

11-47306956-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306956
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306955
    reference: chr 11
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2412-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.121-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2283-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2412-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2283-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2412-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2412-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.136delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2283-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2412-45delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2283-45delC
  variant of: http://identifiers.org/hgnc/6766
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14732
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: TC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-47306965-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306965
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306965
    reference: chr 11
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.144C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2283-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2283-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2283-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2412-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2412-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2412-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2283-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2412-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.121-37C>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2412-37C>A
  variant of: http://identifiers.org/hgnc/6766
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14731
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

11-47306969-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306969
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306969
    reference: chr 11
allele count: 6
allele frequency: 4.967051889135402e-5
allele num: 120796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2412-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2412-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.121-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2283-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2412-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2283-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2412-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2283-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2283-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2412-33C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.148C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14731
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3590
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5361
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-47306975-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306976
    reference: chr 11
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2412-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.121-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2283-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2283-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.155dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2412-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2412-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2283-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2412-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2412-26dupA
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2283-26dupA
  variant of: http://identifiers.org/hgnc/6766
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14729
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5817
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-47306993-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47306993
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47306993
    reference: chr 11
allele count: 18
allele frequency: 1.486325802615933e-4
allele num: 121104
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2283-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2283-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.121-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2283-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2412-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2412-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2412-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.172G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2412-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2412-9G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2283-9G>A
  variant of: http://identifiers.org/hgnc/6766
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14731
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

11-47307003-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307003
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307003
    reference: chr 11
allele count: 5
allele frequency: 4.125208323020312e-5
allele num: 121206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.122G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2413G>T
  hgvsp: ENSP00000384287.2:p.Ala805Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2284G>T
  hgvsp: ENSP00000384204.3:p.Ala762Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2284G>T
  hgvsp: ENSP00000385585.1:p.Ala762Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2413G>T
  hgvsp: ENSP00000304505.6:p.Ala805Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2413G>T
  hgvsp: ENSP00000310933.4:p.Ala805Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2284G>T
  hgvsp: ENSP00000384435.1:p.Ala762Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2413G>T
  hgvsp: ENSP00000343902.4:p.Ala805Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2413G>T
  hgvsp: ENSP00000378745.3:p.Ala805Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.182G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2284G>T
  hgvsp: ENSP00000378753.3:p.Ala762Ser
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4461
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14725
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1387
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala805Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/11-47307008-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307008
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307008
    reference: chr 11
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2418A>C
  hgvsp: ENSP00000304505.6:p.Gln806His
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2418A>C
  hgvsp: ENSP00000384287.2:p.Gln806His
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2289A>C
  hgvsp: ENSP00000378753.3:p.Gln763His
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2289A>C
  hgvsp: ENSP00000385585.1:p.Gln763His
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.127A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2289A>C
  hgvsp: ENSP00000384204.3:p.Gln763His
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2418A>C
  hgvsp: ENSP00000378745.3:p.Gln806His
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.187A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2418A>C
  hgvsp: ENSP00000310933.4:p.Gln806His
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2418A>C
  hgvsp: ENSP00000343902.4:p.Gln806His
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2289A>C
  hgvsp: ENSP00000384435.1:p.Gln763His
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14721
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln806His
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

11-47307018-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307018
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307018
    reference: chr 11
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2428C>T
  hgvsp: ENSP00000343902.4:p.Arg810Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2299C>T
  hgvsp: ENSP00000384204.3:p.Arg767Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2428C>T
  hgvsp: ENSP00000378745.3:p.Arg810Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.137C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2299C>T
  hgvsp: ENSP00000385585.1:p.Arg767Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2428C>T
  hgvsp: ENSP00000304505.6:p.Arg810Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2428C>T
  hgvsp: ENSP00000310933.4:p.Arg810Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2428C>T
  hgvsp: ENSP00000384287.2:p.Arg810Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2299C>T
  hgvsp: ENSP00000384435.1:p.Arg767Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.197C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2299C>T
  hgvsp: ENSP00000378753.3:p.Arg767Trp
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg810Trp
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-47307019-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307019
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307019
    reference: chr 11
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2300G>T
  hgvsp: ENSP00000385585.1:p.Arg767Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2300G>T
  hgvsp: ENSP00000384204.3:p.Arg767Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.198G>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2300G>T
  hgvsp: ENSP00000384435.1:p.Arg767Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2429G>T
  hgvsp: ENSP00000384287.2:p.Arg810Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2429G>T
  hgvsp: ENSP00000378745.3:p.Arg810Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2429G>T
  hgvsp: ENSP00000304505.6:p.Arg810Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2429G>T
  hgvsp: ENSP00000343902.4:p.Arg810Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2429G>T
  hgvsp: ENSP00000310933.4:p.Arg810Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2300G>T
  hgvsp: ENSP00000378753.3:p.Arg767Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.138G>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3268
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3602
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg810Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-47307042-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307042
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307042
    reference: chr 11
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2452A>G
  hgvsp: ENSP00000378745.3:p.Ser818Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2323A>G
  hgvsp: ENSP00000385585.1:p.Ser775Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2323A>G
  hgvsp: ENSP00000384435.1:p.Ser775Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2323A>G
  hgvsp: ENSP00000378753.3:p.Ser775Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2452A>G
  hgvsp: ENSP00000384287.2:p.Ser818Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.221A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2452A>G
  hgvsp: ENSP00000304505.6:p.Ser818Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2452A>G
  hgvsp: ENSP00000310933.4:p.Ser818Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.161A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2452A>G
  hgvsp: ENSP00000343902.4:p.Ser818Gly
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2323A>G
  hgvsp: ENSP00000384204.3:p.Ser775Gly
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3722
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser818Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

11-47307048-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307048
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307048
    reference: chr 11
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2458T>G
  hgvsp: ENSP00000378745.3:p.Ser820Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2458T>G
  hgvsp: ENSP00000343902.4:p.Ser820Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2329T>G
  hgvsp: ENSP00000384204.3:p.Ser777Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.167T>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.227T>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2458T>G
  hgvsp: ENSP00000304505.6:p.Ser820Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2458T>G
  hgvsp: ENSP00000310933.4:p.Ser820Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2329T>G
  hgvsp: ENSP00000384435.1:p.Ser777Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2329T>G
  hgvsp: ENSP00000385585.1:p.Ser777Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2329T>G
  hgvsp: ENSP00000378753.3:p.Ser777Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2458T>G
  hgvsp: ENSP00000384287.2:p.Ser820Ala
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14718
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser820Ala
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ

11-47307052-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307052
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307052
    reference: chr 11
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2333A>T
  hgvsp: ENSP00000384204.3:p.Asp778Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2462A>T
  hgvsp: ENSP00000310933.4:p.Asp821Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2333A>T
  hgvsp: ENSP00000384435.1:p.Asp778Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2462A>T
  hgvsp: ENSP00000384287.2:p.Asp821Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2462A>T
  hgvsp: ENSP00000378745.3:p.Asp821Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2333A>T
  hgvsp: ENSP00000385585.1:p.Asp778Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.171A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2462A>T
  hgvsp: ENSP00000343902.4:p.Asp821Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2333A>T
  hgvsp: ENSP00000378753.3:p.Asp778Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2462A>T
  hgvsp: ENSP00000304505.6:p.Asp821Val
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.231A>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14718
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp821Val
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-47307069-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307069
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307069
    reference: chr 11
allele count: 9
allele frequency: 7.423170188548523e-5
allele num: 121242
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2350C>T
  hgvsp: ENSP00000378753.3:p.Arg784Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2479C>T
  hgvsp: ENSP00000304505.6:p.Arg827Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2350C>T
  hgvsp: ENSP00000384204.3:p.Arg784Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.248C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2479C>T
  hgvsp: ENSP00000343902.4:p.Arg827Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2479C>T
  hgvsp: ENSP00000384287.2:p.Arg827Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2350C>T
  hgvsp: ENSP00000384435.1:p.Arg784Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.188C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2479C>T
  hgvsp: ENSP00000310933.4:p.Arg827Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2350C>T
  hgvsp: ENSP00000385585.1:p.Arg784Trp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2479C>T
  hgvsp: ENSP00000378745.3:p.Arg827Trp
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg827Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

11-47307070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307070
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307070
    reference: chr 11
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2480G>A
  hgvsp: ENSP00000384287.2:p.Arg827Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2480G>A
  hgvsp: ENSP00000343902.4:p.Arg827Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2351G>A
  hgvsp: ENSP00000385585.1:p.Arg784Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2351G>A
  hgvsp: ENSP00000384204.3:p.Arg784Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2351G>A
  hgvsp: ENSP00000378753.3:p.Arg784Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2480G>A
  hgvsp: ENSP00000304505.6:p.Arg827Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2480G>A
  hgvsp: ENSP00000310933.4:p.Arg827Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.189G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2480G>A
  hgvsp: ENSP00000378745.3:p.Arg827Gln
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.249G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2351G>A
  hgvsp: ENSP00000384435.1:p.Arg784Gln
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14711
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg827Gln
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-47307076-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307076
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307076
    reference: chr 11
allele count: 1
allele frequency: 8.249872126982032e-6
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2357G>A
  hgvsp: ENSP00000378753.3:p.Ser786Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2357G>A
  hgvsp: ENSP00000384204.3:p.Ser786Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.195G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2486G>A
  hgvsp: ENSP00000343902.4:p.Ser829Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2486G>A
  hgvsp: ENSP00000378745.3:p.Ser829Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2357G>A
  hgvsp: ENSP00000384435.1:p.Ser786Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2486G>A
  hgvsp: ENSP00000384287.2:p.Ser829Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2486G>A
  hgvsp: ENSP00000304505.6:p.Ser829Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2486G>A
  hgvsp: ENSP00000310933.4:p.Ser829Asn
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.255G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2357G>A
  hgvsp: ENSP00000385585.1:p.Ser786Asn
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14711
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser829Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

11-47307085-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307085
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307085
    reference: chr 11
allele count: 8
allele frequency: 6.603711285742587e-5
allele num: 121144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.204A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2495A>G
  hgvsp: ENSP00000343902.4:p.Asn832Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2495A>G
  hgvsp: ENSP00000310933.4:p.Asn832Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2366A>G
  hgvsp: ENSP00000384435.1:p.Asn789Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.264A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2495A>G
  hgvsp: ENSP00000378745.3:p.Asn832Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2366A>G
  hgvsp: ENSP00000384204.3:p.Asn789Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2495A>G
  hgvsp: ENSP00000304505.6:p.Asn832Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2366A>G
  hgvsp: ENSP00000385585.1:p.Asn789Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2495A>G
  hgvsp: ENSP00000384287.2:p.Asn832Ser
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2366A>G
  hgvsp: ENSP00000378753.3:p.Asn789Ser
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14710
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn832Ser
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

11-47307092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307092
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307092
    reference: chr 11
allele count: 7
allele frequency: 5.780537755169452e-5
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2373C>T
  hgvsp: ENST00000402799.1:c.2373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2502C>T
  hgvsp: ENST00000349238.3:c.2502C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.211C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2373C>T
  hgvsp: ENST00000395344.3:c.2373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2502C>T
  hgvsp: ENST00000311027.5:c.2502C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2502C>T
  hgvsp: ENST00000402192.2:c.2502C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2373C>T
  hgvsp: ENST00000407859.3:c.2373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2373C>T
  hgvsp: ENST00000406482.1:c.2373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.271C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2502C>T
  hgvsp: ENST00000395336.3:c.2502C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2502C>T
  hgvsp: ENST00000342922.4:c.2502C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14703
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1938
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4467
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr834Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

11-47307093-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307093
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307093
    reference: chr 11
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.212G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2503G>A
  hgvsp: ENSP00000378745.3:p.Val835Ile
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2374G>A
  hgvsp: ENSP00000378753.3:p.Val792Ile
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2374G>A
  hgvsp: ENSP00000385585.1:p.Val792Ile
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2503G>A
  hgvsp: ENSP00000343902.4:p.Val835Ile
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2374G>A
  hgvsp: ENSP00000384435.1:p.Val792Ile
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2374G>A
  hgvsp: ENSP00000384204.3:p.Val792Ile
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2503G>A
  hgvsp: ENSP00000304505.6:p.Val835Ile
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2503G>A
  hgvsp: ENSP00000384287.2:p.Val835Ile
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.272G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2503G>A
  hgvsp: ENSP00000310933.4:p.Val835Ile
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14696
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val835Ile
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

11-47307108-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307108
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307108
    reference: chr 11
allele count: 2
allele frequency: 1.654944145635085e-5
allele num: 120850
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.227A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2518A>G
  hgvsp: ENSP00000384287.2:p.Thr840Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2518A>G
  hgvsp: ENSP00000310933.4:p.Thr840Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.287A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2518A>G
  hgvsp: ENSP00000304505.6:p.Thr840Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2518A>G
  hgvsp: ENSP00000343902.4:p.Thr840Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2389A>G
  hgvsp: ENSP00000384204.3:p.Thr797Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2518A>G
  hgvsp: ENSP00000378745.3:p.Thr840Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2389A>G
  hgvsp: ENSP00000378753.3:p.Thr797Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2389A>G
  hgvsp: ENSP00000384435.1:p.Thr797Ala
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2389A>G
  hgvsp: ENSP00000385585.1:p.Thr797Ala
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14695
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr840Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

11-47307110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307110
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307110
    reference: chr 11
allele count: 3
allele frequency: 2.484307457890989e-5
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2520C>T
  hgvsp: ENST00000402192.2:c.2520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2391C>T
  hgvsp: ENST00000407859.3:c.2391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2520C>T
  hgvsp: ENST00000311027.5:c.2520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2520C>T
  hgvsp: ENST00000349238.3:c.2520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2520C>T
  hgvsp: ENST00000395336.3:c.2520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2391C>T
  hgvsp: ENST00000406482.1:c.2391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2391C>T
  hgvsp: ENST00000402799.1:c.2391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2520C>T
  hgvsp: ENST00000342922.4:c.2520C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.229C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.289C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2391C>T
  hgvsp: ENST00000395344.3:c.2391C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14693
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr840Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum

11-47307111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307111
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307111
    reference: chr 11
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.230G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.290G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2392G>A
  hgvsp: ENSP00000385585.1:p.Glu798Lys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2521G>A
  hgvsp: ENSP00000304505.6:p.Glu841Lys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2392G>A
  hgvsp: ENSP00000378753.3:p.Glu798Lys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2521G>A
  hgvsp: ENSP00000343902.4:p.Glu841Lys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2521G>A
  hgvsp: ENSP00000378745.3:p.Glu841Lys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2521G>A
  hgvsp: ENSP00000310933.4:p.Glu841Lys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2392G>A
  hgvsp: ENSP00000384204.3:p.Glu798Lys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2521G>A
  hgvsp: ENSP00000384287.2:p.Glu841Lys
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2392G>A
  hgvsp: ENSP00000384435.1:p.Glu798Lys
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14691
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu841Lys
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

11-47307119-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307119
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307119
    reference: chr 11
allele count: 3
allele frequency: 2.487727212418734e-5
allele num: 120592
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2529C>T
  hgvsp: ENST00000311027.5:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.238C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2400C>T
  hgvsp: ENST00000395344.3:c.2400C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2400C>T
  hgvsp: ENST00000407859.3:c.2400C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2529C>T
  hgvsp: ENST00000349238.3:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2529C>T
  hgvsp: ENST00000395336.3:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2529C>T
  hgvsp: ENST00000402192.2:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2529C>T
  hgvsp: ENST00000342922.4:c.2529C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2400C>T
  hgvsp: ENST00000406482.1:c.2400C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.298C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2400C>T
  hgvsp: ENST00000402799.1:c.2400C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14693
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe843Phe
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

11-47307120-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307120
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307120
    reference: chr 11
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2530G>A
  hgvsp: ENSP00000384287.2:p.Gly844Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2401G>A
  hgvsp: ENSP00000378753.3:p.Gly801Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2530G>A
  hgvsp: ENSP00000343902.4:p.Gly844Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2401G>A
  hgvsp: ENSP00000385585.1:p.Gly801Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2530G>A
  hgvsp: ENSP00000304505.6:p.Gly844Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2401G>A
  hgvsp: ENSP00000384435.1:p.Gly801Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2530G>A
  hgvsp: ENSP00000378745.3:p.Gly844Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.239G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2401G>A
  hgvsp: ENSP00000384204.3:p.Gly801Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2530G>A
  hgvsp: ENSP00000310933.4:p.Gly844Arg
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.299G>A
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14690
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly844Arg
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

11-47307124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307124
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307124
    reference: chr 11
allele count: 1
allele frequency: 8.295726041943191e-6
allele num: 120544
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2534G>A
  hgvsp: ENSP00000378745.3:p.Gly845Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2534G>A
  hgvsp: ENSP00000343902.4:p.Gly845Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2534G>A
  hgvsp: ENSP00000310933.4:p.Gly845Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2534G>A
  hgvsp: ENSP00000384287.2:p.Gly845Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2405G>A
  hgvsp: ENSP00000384204.3:p.Gly802Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2405G>A
  hgvsp: ENSP00000378753.3:p.Gly802Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2534G>A
  hgvsp: ENSP00000304505.6:p.Gly845Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2405G>A
  hgvsp: ENSP00000385585.1:p.Gly802Asp
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.303G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.243G>A
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2405G>A
  hgvsp: ENSP00000384435.1:p.Gly802Asp
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly845Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

11-47307132-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307132
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307132
    reference: chr 11
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2542T>C
  hgvsp: ENSP00000343902.4:p.Ser848Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2542T>C
  hgvsp: ENSP00000384287.2:p.Ser848Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2542T>C
  hgvsp: ENSP00000310933.4:p.Ser848Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2542T>C
  hgvsp: ENSP00000378745.3:p.Ser848Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2413T>C
  hgvsp: ENSP00000385585.1:p.Ser805Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2413T>C
  hgvsp: ENSP00000384204.3:p.Ser805Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2542T>C
  hgvsp: ENSP00000304505.6:p.Ser848Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2413T>C
  hgvsp: ENSP00000378753.3:p.Ser805Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2413T>C
  hgvsp: ENSP00000384435.1:p.Ser805Pro
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.311T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.251T>C
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4805
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser848Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

11-47307135-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307135
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307135
    reference: chr 11
allele count: 1
allele frequency: 8.304958059961797e-6
allele num: 120410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2416T>C
  hgvsp: ENSP00000384204.3:p.Phe806Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.314T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2545T>C
  hgvsp: ENSP00000343902.4:p.Phe849Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2416T>C
  hgvsp: ENSP00000385585.1:p.Phe806Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2545T>C
  hgvsp: ENSP00000384287.2:p.Phe849Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2416T>C
  hgvsp: ENSP00000378753.3:p.Phe806Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.254T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2545T>C
  hgvsp: ENSP00000304505.6:p.Phe849Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2545T>C
  hgvsp: ENSP00000378745.3:p.Phe849Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2416T>C
  hgvsp: ENSP00000384435.1:p.Phe806Leu
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2545T>C
  hgvsp: ENSP00000310933.4:p.Phe849Leu
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14689
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe849Leu
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

11-47307149-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307149
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307149
    reference: chr 11
allele count: 1
allele frequency: 8.320436656515735e-6
allele num: 120186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+8C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+8C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3212
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2551+8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

11-47307158-G-GTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307158
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307160
    reference: chr 11
allele count: 1
allele frequency: 8.329446258412741e-6
allele num: 120056
alternate allele: GTC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+24_260+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+24_2551+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+24_2422+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+24_2422+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+24_2422+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+24_2551+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+24_2551+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+24_320+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+24_2551+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+24_2551+25dupTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+24_2422+25dupTC
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14687
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

11-47307158-GTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307158
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307156
    reference: chr 11
allele count: 1
allele frequency: 8.329446258412741e-6
allele num: 120056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+24_2422+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+24_2551+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+24_2551+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+24_260+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+24_2422+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+24_2551+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+24_2422+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+24_2422+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+24_320+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+24_2551+25delTC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+24_2551+25delTC
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14687
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: GTC
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

11-47307160-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307160
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307160
    reference: chr 11
allele count: 1
allele frequency: 8.331944675887353e-6
allele num: 120020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+19C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+19C>G
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14686
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-47307162-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307162
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307162
    reference: chr 11
allele count: 1
allele frequency: 8.332916687498959e-6
allele num: 120006
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+21C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+21C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3730
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14686
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

11-47307164-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307164
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307164
    reference: chr 11
allele count: 1
allele frequency: 8.335278231587371e-6
allele num: 119972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+23C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+23C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14685
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4991
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-47307167-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307167
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307167
    reference: chr 11
allele count: 4
allele frequency: 3.33683701219614e-5
allele num: 119874
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+26A>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+26A>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3858
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14685
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

11-47307169-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307169
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307168
    reference: chr 11
allele count: 1
allele frequency: 8.340144451301897e-6
allele num: 119902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+30delC
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+30delC
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14683
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: TC
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-47307170-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307170
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307170
    reference: chr 11
allele count: 11
allele frequency: 9.176148686976543e-5
allele num: 119876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+29C>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+29C>G
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14682
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 2
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-47307180-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307180
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307180
    reference: chr 11
allele count: 1
allele frequency: 8.349475652928997e-6
allele num: 119768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+39A>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+39A>C
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14682
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

11-47307180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307180
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307180
    reference: chr 11
allele count: 1
allele frequency: 8.349475652928997e-6
allele num: 119768
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2551+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2551+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2551+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2422+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2551+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2422+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2551+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2422+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.320+39A>G
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2422+39A>G
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14682
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3860
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50101
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

11-47307943-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307943
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307943
    reference: chr 11
allele count: 4
allele frequency: 3.305566574110803e-5
allele num: 121008
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2552-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+802T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2423-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2423-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2423-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2552-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2552-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2552-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2552-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2423-41T>C
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.321-41T>C
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

11-47307945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 47307945
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 47307945
    reference: chr 11
allele count: 12
allele frequency: 9.919486831881231e-5
allele num: 120974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384435
  ensembl transcript: ENST00000406482
  gene symbol: MADD
  hgvsc: ENST00000406482.1:c.2423-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000343902
  ensembl transcript: ENST00000342922
  gene symbol: MADD
  hgvsc: ENST00000342922.4:c.2552-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000310933
  ensembl transcript: ENST00000311027
  gene symbol: MADD
  hgvsc: ENST00000311027.5:c.2552-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524530
  gene symbol: MADD
  hgvsc: ENST00000524530.1:n.260+804C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384204
  ensembl transcript: ENST00000407859
  gene symbol: MADD
  hgvsc: ENST00000407859.3:c.2423-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl transcript: ENST00000524686
  gene symbol: MADD
  hgvsc: ENST00000524686.1:n.321-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378753
  ensembl transcript: ENST00000395344
  gene symbol: MADD
  hgvsc: ENST00000395344.3:c.2423-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000304505
  ensembl transcript: ENST00000349238
  gene symbol: MADD
  hgvsc: ENST00000349238.3:c.2552-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000378745
  ensembl transcript: ENST00000395336
  gene symbol: MADD
  hgvsc: ENST00000395336.3:c.2552-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000384287
  ensembl transcript: ENST00000402192
  gene symbol: MADD
  hgvsc: ENST00000402192.2:c.2552-39C>T
  variant of: http://identifiers.org/hgnc/6766
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110514
  ensembl protein: ENSP00000385585
  ensembl transcript: ENST00000402799
  gene symbol: MADD
  hgvsc: ENST00000402799.1:c.2423-39C>T
  variant of: http://identifiers.org/hgnc/6766
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6196
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1958
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5406
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9941
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3949
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4652
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.99e0

FS
type: SiteQuality
SIO_000300: 6.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.845628e6

MQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.385e0

QD
type: SiteQuality
SIO_000300: 1.401e1

VQSLOD
type: SiteQuality
SIO_000300: -1.026e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

GenotypeQuality
all individuals: 3945
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9933
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4650
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30570
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5406
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.845594e6

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 1.679e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.69e0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3940
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5404
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4644
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3054
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9932
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500195025353296e-5
allele num: 66658
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.129e0

QD
type: SiteQuality
SIO_000300: 1.527e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

DP
type: SiteQuality
SIO_000300: 1.844818e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.12e-1

FS
type: SiteQuality
SIO_000300: 1.1119e1

VQSLOD
type: SiteQuality
SIO_000300: -1.562e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9912
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30488
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5396
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1678
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3051
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.19e-1

MQ
type: SiteQuality
SIO_000300: 6.022e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.803e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

DP
type: SiteQuality
SIO_000300: 1.843758e6

QD
type: SiteQuality
SIO_000300: 1.015e1

GenotypeQuality
all individuals: 30544
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3051
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9917
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5392
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3931
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1678
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.72e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.128e0

DP
type: SiteQuality
SIO_000300: 1.843538e6

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.8e-1

GenotypeQuality
all individuals: 0
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30488
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4636
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9904
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3052
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5390
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 1262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.942837306179125e-4
allele num: 8642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 2.85e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: -4.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -4.827e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e-1

DP
type: SiteQuality
SIO_000300: 1.84266e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.52e-1

QD
type: SiteQuality
SIO_000300: 9.6e0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9907
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1677
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4635
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30512
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3929
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3054
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

African
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South Asian
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Other
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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MQRankSum
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QD
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 10388
num of homozygotes: 0

InbreedingCoeff
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QD
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.503668952243474e-5
allele num: 66504
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Other
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ClippingRankSum
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SIO_000300: 5.02e-1

MQRankSum
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FS
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SIO_000300: 0.0e0

BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 5
allele frequency: 7.51834476121737e-5
allele num: 66504
num of homozygotes: 0

South Asian
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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DP
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SIO_000300: 1.836031e6

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.972e1

ClippingRankSum
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SIO_000300: 5.02e-1

FS
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 1.513317191283293e-4
allele num: 6608
num of homozygotes: 0

East Asian
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66504
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Latino
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num of homozygotes: 0

Other
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DP
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BaseQRankSum
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QD
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InbreedingCoeff
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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Other
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MQ
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DP
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FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Finnish)
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East Asian
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Other
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South Asian
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African
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European (Non-Finnish)
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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MQ
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MQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

European (Finnish)
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African
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Other
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East Asian
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European (Non-Finnish)
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South Asian
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QD
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5308
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507613447911955e-5
allele num: 66330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

DP
type: SiteQuality
SIO_000300: 1.819811e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.025e0

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

FS
type: SiteQuality
SIO_000300: 3.123e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.596e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
all individuals: 2891
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 9

South Asian
type: Population
allele count: 6
allele frequency: 3.717011522735721e-4
allele num: 16142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031772980839195e-5
allele num: 65968
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

MQRankSum
type: SiteQuality
SIO_000300: -9.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.72e-1

FS
type: SiteQuality
SIO_000300: 1.514e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 1.774587e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

QD
type: SiteQuality
SIO_000300: 1.406e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4262
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GenotypeQuality
all individuals: 1830
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.232082762059081e-5
allele num: 16046
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517220452131695e-5
allele num: 65910
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

FS
type: SiteQuality
SIO_000300: 4.019e0

DP
type: SiteQuality
SIO_000300: 1.76579e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 1.256e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.93e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1605
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variant carriers: 0

GenotypeQuality
all individuals: 2852
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.554010565304512e-5
allele num: 65876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.825e0

FS
type: SiteQuality
SIO_000300: 3.53e0

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.146e1

MQ
type: SiteQuality
SIO_000300: 5.915e1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 1.763148e6

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 14
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 5260
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2852
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variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16058
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.036007043536341e-5
allele num: 65876
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.14e-1

DP
type: SiteQuality
SIO_000300: 1.763148e6

FS
type: SiteQuality
SIO_000300: 3.53e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

QD
type: SiteQuality
SIO_000300: 1.146e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.825e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15762
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.17096018735363e-4
allele num: 8540
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

QD
type: SiteQuality
SIO_000300: 1.617e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

FS
type: SiteQuality
SIO_000300: 1.423e0

DP
type: SiteQuality
SIO_000300: 1.71903e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.487e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15632
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65532
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171508903467666e-4
allele num: 8536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.4355e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.703027e6

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.647e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.580432392817882e-5
allele num: 65496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 9.91e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -1.642e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

DP
type: SiteQuality
SIO_000300: 1.691393e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 8
allele frequency: 6.991784653032686e-4
allele num: 11442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10158
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15532
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.15e-1

FS
type: SiteQuality
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MQRankSum
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SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.727e0

DP
type: SiteQuality
SIO_000300: 1.682793e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.59e-1

QD
type: SiteQuality
SIO_000300: 1.201e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529285823520416e-5
allele num: 65390
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

DP
type: SiteQuality
SIO_000300: 1.67087e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -2.055e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

BaseQRankSum
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SIO_000300: -6.39e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65282
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.521455588887439e-5
allele num: 15334
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.636839e6

QD
type: SiteQuality
SIO_000300: 2.831e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.929e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.752e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64924
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.758705592683785e-4
allele num: 11372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14878
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.263e0

DP
type: SiteQuality
SIO_000300: 1.589894e6

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e0

QD
type: SiteQuality
SIO_000300: 1.758e1

VQSLOD
type: SiteQuality
SIO_000300: -6.327e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.620218074293107e-5
allele num: 64932
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.586266e6

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

MQRankSum
type: SiteQuality
SIO_000300: 5.31e-1

QD
type: SiteQuality
SIO_000300: 1.666e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.17e-1

FS
type: SiteQuality
SIO_000300: 1.219e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.542686125080991e-5
allele num: 64822
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14804
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

QD
type: SiteQuality
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MQ
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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SIO_000300: -4.16e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506841058405159e-5
allele num: 66364
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66360
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 6.110228522546743e-5
allele num: 16366
num of homozygotes: 0

African
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Other
type: Population
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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DP
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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MQRankSum
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FS
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50115
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.99e0

MQRankSum
type: SiteQuality
SIO_000300: 7.86e-1

FS
type: SiteQuality
SIO_000300: 2.582e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.541485e6

QD
type: SiteQuality
SIO_000300: 2.71e1

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50117
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 104
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.659875564230816e-4
allele num: 16394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.8e-1

DP
type: SiteQuality
SIO_000300: 4.544673e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

QD
type: SiteQuality
SIO_000300: 1.439e1

VQSLOD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.476e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

GenotypeQuality
all individuals: 517
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50114
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1306
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504573904670197e-5
allele num: 66464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.843e0

QD
type: SiteQuality
SIO_000300: 1.476e1

MQ
type: SiteQuality
SIO_000300: 6.1e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.548e0

FS
type: SiteQuality
SIO_000300: 1.336e0

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: 2.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-1

DP
type: SiteQuality
SIO_000300: 4.548422e6

GenotypeQuality
all individuals: 164
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6291
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50124
bin: 9.75e1
variant carriers: 18

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1362
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.091305929428883e-3
allele num: 16494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.555471e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.656e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.74e-1

FS
type: SiteQuality
SIO_000300: 5.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.16e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

GenotypeDepth
all individuals: 3269
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1937
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4799
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1381
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50113
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 596
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6430
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002462018855461e-5
allele num: 66612
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.039999999999999e-2

DP
type: SiteQuality
SIO_000300: 4.557027e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.435e0

VQSLOD
type: SiteQuality
SIO_000300: -1.23e0

QD
type: SiteQuality
SIO_000300: 1.295e1

GenotypeDepth
all individuals: 1385
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6515
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50113
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.57e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.557486e6

MQRankSum
type: SiteQuality
SIO_000300: 8.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 14720
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50113
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6588
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 4.55877e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

FS
type: SiteQuality
SIO_000300: 1.743e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.253e0

QD
type: SiteQuality
SIO_000300: 1.071e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 3722
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50112
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 6624
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1391
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.975e1

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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BaseQRankSum
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SIO_000300: 1.21e0

FS
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SIO_000300: 5.35e-1

VQSLOD
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QD
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SIO_000300: 1.402e1

DP
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SIO_000300: 4.558664e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
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allele num: 10402
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South Asian
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.35e-1

DP
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VQSLOD
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ReadPosRankSum
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SIO_000300: 1.17e0

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.46e0

QD
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SIO_000300: 1.579e1

MQ
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SIO_000300: 5.935e1

BaseQRankSum
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SIO_000300: 4.45e0

ClippingRankSum
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SIO_000300: 1.87e-1

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
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VQSLOD
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ClippingRankSum
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SIO_000300: 4.96e-1

FS
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SIO_000300: 2.602e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.558973e6

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
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SIO_000300: 3.1e-1

FS
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BaseQRankSum
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QD
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ReadPosRankSum
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SIO_000300: 2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.34e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e0

GenotypeDepth
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variant carriers: 9

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 9

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
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allele count: 9
allele frequency: 1.041184636742249e-3
allele num: 8644
num of homozygotes: 0

Other
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BaseQRankSum
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SIO_000300: -1.291e0

ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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QD
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MQRankSum
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SIO_000300: -2.24e-1

ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66652
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MQ
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SIO_000300: 5.934e1

ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

Other
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African
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Latino
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European (Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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FS
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QD
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MQ
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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Latino
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East Asian
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South Asian
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ReadPosRankSum
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DP
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MQRankSum
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QD
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SIO_000300: 1.307e1

FS
type: SiteQuality
SIO_000300: 1.095e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.84e0

VQSLOD
type: SiteQuality
SIO_000300: 2.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.81e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

South Asian
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allele frequency: 1.213592233009709e-4
allele num: 16480
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 5
allele frequency: 4.84214603912454e-4
allele num: 10326
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e0

VQSLOD
type: SiteQuality
SIO_000300: 5.37e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.552723e6

ReadPosRankSum
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SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 1.094e0

QD
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BaseQRankSum
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SIO_000300: 5.2e-1

VQSLOD
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SIO_000300: 1.02e0

MQRankSum
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SIO_000300: -7.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.938e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 2.316423442205235e-4
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.72e-1

VQSLOD
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SIO_000300: 3.93e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 4.550115e6

InbreedingCoeff
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SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.66e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 2.317497103128621e-4
allele num: 8630
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Other
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South Asian
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allele frequency: 6.072382803011902e-5
allele num: 16468
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
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VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.785e0

QD
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66354
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 2.605071205279611e-4
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
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allele num: 66268
num of homozygotes: 0

South Asian
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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DP
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MQRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele num: 10222
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East Asian
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South Asian
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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QD
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MQ
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509844184080203e-5
allele num: 66232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10220
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.908e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.348e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 7.157e0

DP
type: SiteQuality
SIO_000300: 4.545641e6

VQSLOD
type: SiteQuality
SIO_000300: -1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 1.051e1

GenotypeDepth
all individuals: 14688
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 609
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511121856866538e-5
allele num: 66176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
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SIO_000300: -7.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

QD
type: SiteQuality
SIO_000300: 1.344e1

FS
type: SiteQuality
SIO_000300: 2.399e0

MQRankSum
type: SiteQuality
SIO_000300: -6.62e-1

DP
type: SiteQuality
SIO_000300: 4.544151e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e-2

GenotypeDepth
all individuals: 4619
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6004
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.178e0

FS
type: SiteQuality
SIO_000300: 6.015e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

DP
type: SiteQuality
SIO_000300: 4.543571e6

QD
type: SiteQuality
SIO_000300: 1.188e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

VQSLOD
type: SiteQuality
SIO_000300: -3.367e-1

GenotypeDepth
all individuals: 14688
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 465
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
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variant carriers: 0

GenotypeQuality
all individuals: 50109
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5655
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.098304671301378e-5
allele num: 16398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.927e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.473e1

DP
type: SiteQuality
SIO_000300: 4.539686e6

MQRankSum
type: SiteQuality
SIO_000300: 9.75e-1

FS
type: SiteQuality
SIO_000300: 5.328e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.9e-2

GenotypeQuality
all individuals: 445
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
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variant carriers: 0

GenotypeQuality
all individuals: 551
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variant carriers: 0

GenotypeQuality
all individuals: 136
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65996
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.709284096847239e-5
allele num: 11482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.632e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 5.25e0

MQRankSum
type: SiteQuality
SIO_000300: 7.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

DP
type: SiteQuality
SIO_000300: 4.535729e6

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515243348081702e-5
allele num: 65996
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.25e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.632e1

ReadPosRankSum
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SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 4.535729e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 494
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variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515794579518584e-5
allele num: 65972
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.534226e6

VQSLOD
type: SiteQuality
SIO_000300: 3.2e-2

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: 3.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.51e-1

QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -1.144e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 74
bin: 4.75e1
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GenotypeQuality
all individuals: 434
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10098
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.110228522546743e-5
allele num: 16366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65970
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.425e0

QD
type: SiteQuality
SIO_000300: 4.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.77e-2

FS
type: SiteQuality
SIO_000300: 1.2626e1

DP
type: SiteQuality
SIO_000300: 4.532628e6

VQSLOD
type: SiteQuality
SIO_000300: -9.821e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQRankSum
type: SiteQuality
SIO_000300: -9.399999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.69e-1

GenotypeQuality
all individuals: 268
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 434
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50107
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65956
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164415463437354e-4
allele num: 8588
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.71e-1

QD
type: SiteQuality
SIO_000300: 1.565e1

FS
type: SiteQuality
SIO_000300: 1.607e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

DP
type: SiteQuality
SIO_000300: 4.531667e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.675e0

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

GenotypeQuality
all individuals: 853
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.552628384120432e-5
allele num: 65896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.119951040391677e-5
allele num: 16340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 8.237e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.78e0

DP
type: SiteQuality
SIO_000300: 4.52924e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 2.02e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50107
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 109
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.916699722332408e-5
allele num: 10084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65912
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.3261e1

QD
type: SiteQuality
SIO_000300: 3.113e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.92e-1

DP
type: SiteQuality
SIO_000300: 4.52703e6

MQ
type: SiteQuality
SIO_000300: 6.035e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.49e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: -1.846e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.8e-1

GenotypeQuality
all individuals: 895
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
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variant carriers: 0

GenotypeQuality
all individuals: 187
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GenotypeQuality
all individuals: 60
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variant carriers: 0

GenotypeQuality
all individuals: 112
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GenotypeQuality
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GenotypeQuality
all individuals: 50114
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 94
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 320
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GenotypeQuality
all individuals: 4597
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.735243693362724e-4
allele num: 16332
num of homozygotes: 2

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65904
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.279e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

MQRankSum
type: SiteQuality
SIO_000300: -2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.26e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

QD
type: SiteQuality
SIO_000300: 1.82e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: -4.841e-1

DP
type: SiteQuality
SIO_000300: 4.526857e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 930
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65846
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.518172e6

VQSLOD
type: SiteQuality
SIO_000300: -7.16e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 1.336e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e0

QD
type: SiteQuality
SIO_000300: 1.386e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518695137138171e-5
allele num: 65846
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.92e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

FS
type: SiteQuality
SIO_000300: 1.336e0

VQSLOD
type: SiteQuality
SIO_000300: -7.16e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.518172e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3139
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GenotypeQuality
all individuals: 3312
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.45398773006135e-4
allele num: 16300
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.93e1

DP
type: SiteQuality
SIO_000300: 2.193452e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 5.590000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
SIO_000300: 1.56e1

MQRankSum
type: SiteQuality
SIO_000300: 6.57e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 160
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variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3310
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14113
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 321
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5024
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.38728323699422e-3
allele num: 8650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

DP
type: SiteQuality
SIO_000300: 2.19509e6

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.818e0