6-131915457-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915457
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915457
    reference: chr 6
allele count: 1
allele frequency: 8.276775368316504e-6
allele num: 120820
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.594T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.3014T>C
  hgvsp: ENSP00000357047.3:p.Leu1005Pro
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.3014T>C
  hgvsp: ENSP00000357039.3:p.Leu1005Pro
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3032T>C
  hgvsp: ENSP00000357037.1:p.Leu1011Pro
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3032T>C
  hgvsp: ENSP00000346588.4:p.Leu1011Pro
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1937T>C
  hgvsp: ENSP00000439977.1:p.Leu646Pro
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3032T>C
  hgvsp: ENSP00000384536.3:p.Leu1011Pro
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33662
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3668
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu1005Pro
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: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

6-131915460-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915460
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915460
    reference: chr 6
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3029A>G
  hgvsp: ENSP00000357037.1:p.Tyr1010Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.3011A>G
  hgvsp: ENSP00000357039.3:p.Tyr1004Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.591A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.3011A>G
  hgvsp: ENSP00000357047.3:p.Tyr1004Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1934A>G
  hgvsp: ENSP00000439977.1:p.Tyr645Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3029A>G
  hgvsp: ENSP00000384536.3:p.Tyr1010Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3029A>G
  hgvsp: ENSP00000346588.4:p.Tyr1010Cys
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7766
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7099
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8708
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr1004Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

6-131915470-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915470
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915470
    reference: chr 6
allele count: 1
allele frequency: 8.313242996092776e-6
allele num: 120290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.3001C>G
  hgvsp: ENSP00000357039.3:p.Pro1001Ala
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3019C>G
  hgvsp: ENSP00000346588.4:p.Pro1007Ala
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.581C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1924C>G
  hgvsp: ENSP00000439977.1:p.Pro642Ala
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.3001C>G
  hgvsp: ENSP00000357047.3:p.Pro1001Ala
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3019C>G
  hgvsp: ENSP00000357037.1:p.Pro1007Ala
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3019C>G
  hgvsp: ENSP00000384536.3:p.Pro1007Ala
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7733
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1915
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3540
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro1001Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

6-131915479-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915479
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915479
    reference: chr 6
allele count: 4
allele frequency: 3.333722267597886e-5
allele num: 119986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-4G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-4G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-4G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-4G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-4G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-4G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-4G>A
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7062
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3475
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33663
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2996-4G>A
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

6-131915486-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915486
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915486
    reference: chr 6
allele count: 2
allele frequency: 1.669644198821231e-5
allele num: 119786
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-11T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-11T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-11T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-11T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-11T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-11T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-11T>C
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3295
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

6-131915487-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915487
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915487
    reference: chr 6
allele count: 2
allele frequency: 1.670397220459025e-5
allele num: 119732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-12T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-12T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-12T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-12T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-12T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-12T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-12T>C
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1299
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-131915493-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915493
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915494
    reference: chr 6
allele count: 1
allele frequency: 8.37548996616302e-6
allele num: 119396
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-19dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-19dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-19dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-19dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-19dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-19dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-19dupT
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3105
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33665
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP

6-131915495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915495
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915495
    reference: chr 6
allele count: 1
allele frequency: 8.382651264942076e-6
allele num: 119294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-20G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-20G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-20G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-20G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-20G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-20G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-20G>A
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7874
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7530
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

6-131915499-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915499
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915499
    reference: chr 6
allele count: 2
allele frequency: 1.679909956826314e-5
allele num: 119054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-24G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-24G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-24G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-24G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-24G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-24G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-24G>A
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7843
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3292
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
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: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

6-131915504-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915504
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915504
    reference: chr 6
allele count: 2
allele frequency: 1.681718043152885e-5
allele num: 118926
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-29A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-29A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-29A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-29A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-29A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-29A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-29A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2018
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33664
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

6-131915505-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915505
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915505
    reference: chr 6
allele count: 5
allele frequency: 4.212867783357487e-5
allele num: 118684
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-30C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-30C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-30C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-30C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-30C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-30C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-30C>T
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33664
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3309
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3093
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

6-131915521-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915521
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915521
    reference: chr 6
allele count: 3
allele frequency: 2.540693439929538e-5
allele num: 118078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-46T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-46T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-46T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-46T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-46T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-46T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-46T>C
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8052
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7676
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7060
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3266
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3257
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6235
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP

6-131915525-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131915525
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131915523
    reference: chr 6
allele count: 1
allele frequency: 8.4870911343846e-6
allele num: 117826
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.576-52_576-51delCA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3014-52_3014-51delCA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2996-52_2996-51delCA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3014-52_3014-51delCA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1919-52_1919-51delCA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3014-52_3014-51delCA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2996-52_2996-51delCA
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5964
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33666
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3085
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3287
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CTG
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

6-131917036-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917036
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917036
    reference: chr 6
allele count: 1
allele frequency: 8.581333882538702e-6
allele num: 116532
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3013+51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2995+51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1918+51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3013+51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.575+51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3013+51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2995+51A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10681
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1908
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23610
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

6-131917052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917052
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917052
    reference: chr 6
allele count: 2
allele frequency: 1.713150140478312e-5
allele num: 116744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.575+35C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2995+35C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3013+35C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1918+35C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3013+35C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3013+35C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2995+35C>T
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7422
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

6-131917053-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917053
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917053
    reference: chr 6
allele count: 1
allele frequency: 8.562523546939755e-6
allele num: 116788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3013+34C>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3013+34C>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3013+34C>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2995+34C>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1918+34C>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.575+34C>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2995+34C>A
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14527
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18800
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1611
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7436
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/6-131917061-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917061
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917061
    reference: chr 6
allele count: 1
allele frequency: 8.532277606184194e-6
allele num: 117202
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2995+26G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3013+26G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3013+26G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.575+26G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1918+26G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3013+26G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2995+26G>T
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1501
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32440
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7524
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-131917061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917061
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917061
    reference: chr 6
allele count: 3
allele frequency: 2.559683281855259e-5
allele num: 117202
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2995+26G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1918+26G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3013+26G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2995+26G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3013+26G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.575+26G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3013+26G>A
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32440
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1528
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

6-131917062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917062
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917062
    reference: chr 6
allele count: 403
allele frequency: 3.434815218873585e-3
allele num: 117328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2995+25C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3013+25C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.575+25C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3013+25C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3013+25C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1918+25C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2995+25C>T
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 5.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 4.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 15309
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 5.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 19660
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 9601
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 4.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 3.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 7
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD

6-131917067-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917067
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917066
    reference: chr 6
allele count: 1
allele frequency: 8.496321092966746e-6
allele num: 117698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2995+19delT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.575+19delT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1918+19delT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3013+19delT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2995+19delT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3013+19delT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3013+19delT
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8833
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33589
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: TA
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ

6-131917072-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917072
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917072
    reference: chr 6
allele count: 3
allele frequency: 2.542372881355932e-5
allele num: 118000
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3013+15A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2995+15A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1918+15A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.575+15A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3013+15A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2995+15A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3013+15A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20155
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9694
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

6-131917094-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917094
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917094
    reference: chr 6
allele count: 1
allele frequency: 8.390106386548982e-6
allele num: 119188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3006A>G
  hgvsp: ENST00000403834.3:c.3006A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1911A>G
  hgvsp: ENST00000545957.1:c.1911A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2988A>G
  hgvsp: ENST00000368060.3:c.2988A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3006A>G
  hgvsp: ENST00000354577.4:c.3006A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2988A>G
  hgvsp: ENST00000368068.3:c.2988A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3006A>G
  hgvsp: ENST00000368058.1:c.3006A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.568A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35175
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys996Lys
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

6-131917098-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917098
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917098
    reference: chr 6
allele count: 1
allele frequency: 8.380122349786308e-6
allele num: 119330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1907A>G
  hgvsp: ENSP00000439977.1:p.Tyr636Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.3002A>G
  hgvsp: ENSP00000384536.3:p.Tyr1001Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.564A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.3002A>G
  hgvsp: ENSP00000346588.4:p.Tyr1001Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2984A>G
  hgvsp: ENSP00000357039.3:p.Tyr995Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2984A>G
  hgvsp: ENSP00000357047.3:p.Tyr995Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.3002A>G
  hgvsp: ENSP00000357037.1:p.Tyr1001Cys
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35292
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7791
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr995Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

6-131917105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917105
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917105
    reference: chr 6
allele count: 2
allele frequency: 1.671709657466691e-5
allele num: 119638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.557G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2995G>A
  hgvsp: ENSP00000384536.3:p.Gly999Ser
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2995G>A
  hgvsp: ENSP00000357037.1:p.Gly999Ser
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2995G>A
  hgvsp: ENSP00000346588.4:p.Gly999Ser
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2977G>A
  hgvsp: ENSP00000357047.3:p.Gly993Ser
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2977G>A
  hgvsp: ENSP00000357039.3:p.Gly993Ser
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1900G>A
  hgvsp: ENSP00000439977.1:p.Gly634Ser
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17030
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3014
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7817
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8841
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly993Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-131917106-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917106
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917106
    reference: chr 6
allele count: 10
allele frequency: 8.356313194618534e-5
allele num: 119670
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1899A>C
  hgvsp: ENST00000545957.1:c.1899A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2994A>C
  hgvsp: ENST00000403834.3:c.2994A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2994A>C
  hgvsp: ENST00000354577.4:c.2994A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2976A>C
  hgvsp: ENST00000368068.3:c.2976A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2994A>C
  hgvsp: ENST00000368058.1:c.2994A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.556A>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2976A>C
  hgvsp: ENST00000368060.3:c.2976A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17027
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35522
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly992Gly
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-131917111-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917111
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917111
    reference: chr 6
allele count: 1
allele frequency: 8.339866228545694e-6
allele num: 119906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.551C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2989C>T
  hgvsp: ENST00000403834.3:c.2989C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1894C>T
  hgvsp: ENST00000545957.1:c.1894C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2971C>T
  hgvsp: ENST00000368068.3:c.2971C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2989C>T
  hgvsp: ENST00000368058.1:c.2989C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2989C>T
  hgvsp: ENST00000354577.4:c.2989C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2971C>T
  hgvsp: ENST00000368060.3:c.2971C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17136
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1517
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35711
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Leu991Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

6-131917145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917145
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917145
    reference: chr 6
allele count: 5
allele frequency: 4.140443855581318e-5
allele num: 120760
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2955G>A
  hgvsp: ENST00000354577.4:c.2955G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.517G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2937G>A
  hgvsp: ENST00000368060.3:c.2937G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2937G>A
  hgvsp: ENST00000368068.3:c.2937G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2955G>A
  hgvsp: ENST00000368058.1:c.2955G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2955G>A
  hgvsp: ENST00000403834.3:c.2955G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1860G>A
  hgvsp: ENST00000545957.1:c.1860G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9866
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro979Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS

6-131917153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917153
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917153
    reference: chr 6
allele count: 2
allele frequency: 1.654013463669594e-5
allele num: 120918
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2947T>C
  hgvsp: ENST00000368058.1:c.2947T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2929T>C
  hgvsp: ENST00000368068.3:c.2929T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2947T>C
  hgvsp: ENST00000403834.3:c.2947T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2947T>C
  hgvsp: ENST00000354577.4:c.2947T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1852T>C
  hgvsp: ENST00000545957.1:c.1852T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2929T>C
  hgvsp: ENST00000368060.3:c.2929T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.509T>C
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36203
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu977Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-131917168-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917168
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917168
    reference: chr 6
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2932C>T
  hgvsp: ENSP00000346588.4:p.His978Tyr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2932C>T
  hgvsp: ENSP00000357037.1:p.His978Tyr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.494C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2914C>T
  hgvsp: ENSP00000357047.3:p.His972Tyr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2914C>T
  hgvsp: ENSP00000357039.3:p.His972Tyr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2932C>T
  hgvsp: ENSP00000384536.3:p.His978Tyr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1837C>T
  hgvsp: ENSP00000439977.1:p.His613Tyr
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His972Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

6-131917175-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917175
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917175
    reference: chr 6
allele count: 2
allele frequency: 1.650519088253256e-5
allele num: 121174
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.487A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2925A>G
  hgvsp: ENSP00000357037.1:p.Ile975Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2925A>G
  hgvsp: ENSP00000346588.4:p.Ile975Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2907A>G
  hgvsp: ENSP00000357047.3:p.Ile969Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1830A>G
  hgvsp: ENSP00000439977.1:p.Ile610Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2925A>G
  hgvsp: ENSP00000384536.3:p.Ile975Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2907A>G
  hgvsp: ENSP00000357039.3:p.Ile969Met
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8840
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile969Met
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

6-131917176-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917176
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917176
    reference: chr 6
allele count: 2
allele frequency: 1.650328415354656e-5
allele num: 121188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1829T>C
  hgvsp: ENSP00000439977.1:p.Ile610Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2906T>C
  hgvsp: ENSP00000357047.3:p.Ile969Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.486T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2924T>C
  hgvsp: ENSP00000357037.1:p.Ile975Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2924T>C
  hgvsp: ENSP00000346588.4:p.Ile975Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2924T>C
  hgvsp: ENSP00000384536.3:p.Ile975Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2906T>C
  hgvsp: ENSP00000357039.3:p.Ile969Thr
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36379
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile969Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

6-131917184-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917184
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917184
    reference: chr 6
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1821A>G
  hgvsp: ENST00000545957.1:c.1821A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2916A>G
  hgvsp: ENST00000354577.4:c.2916A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2898A>G
  hgvsp: ENST00000368060.3:c.2898A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2916A>G
  hgvsp: ENST00000368058.1:c.2916A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.478A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2898A>G
  hgvsp: ENST00000368068.3:c.2898A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2916A>G
  hgvsp: ENST00000403834.3:c.2916A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8838
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36421
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val966Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP

6-131917187-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917187
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917187
    reference: chr 6
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2913A>G
  hgvsp: ENST00000354577.4:c.2913A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2913A>G
  hgvsp: ENST00000368058.1:c.2913A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2913A>G
  hgvsp: ENST00000403834.3:c.2913A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2895A>G
  hgvsp: ENST00000368060.3:c.2895A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.475A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2895A>G
  hgvsp: ENST00000368068.3:c.2895A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1818A>G
  hgvsp: ENST00000545957.1:c.1818A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7895
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro965Pro
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

6-131917208-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917208
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917208
    reference: chr 6
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1797T>C
  hgvsp: ENST00000545957.1:c.1797T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2874T>C
  hgvsp: ENST00000368060.3:c.2874T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2892T>C
  hgvsp: ENST00000368058.1:c.2892T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2892T>C
  hgvsp: ENST00000403834.3:c.2892T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2874T>C
  hgvsp: ENST00000368068.3:c.2874T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2892T>C
  hgvsp: ENST00000354577.4:c.2892T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.454T>C
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7899
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36486
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1521
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn958Asn
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-131917218-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917218
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917218
    reference: chr 6
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2864A>G
  hgvsp: ENSP00000357047.3:p.Tyr955Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2882A>G
  hgvsp: ENSP00000384536.3:p.Tyr961Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2882A>G
  hgvsp: ENSP00000357037.1:p.Tyr961Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.444A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2864A>G
  hgvsp: ENSP00000357039.3:p.Tyr955Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1787A>G
  hgvsp: ENSP00000439977.1:p.Tyr596Cys
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2882A>G
  hgvsp: ENSP00000346588.4:p.Tyr961Cys
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2015
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2383
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr955Cys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-131917220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917220
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917220
    reference: chr 6
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2862C>T
  hgvsp: ENST00000368068.3:c.2862C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2880C>T
  hgvsp: ENST00000403834.3:c.2880C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2880C>T
  hgvsp: ENST00000368058.1:c.2880C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2880C>T
  hgvsp: ENST00000354577.4:c.2880C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2862C>T
  hgvsp: ENST00000368060.3:c.2862C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.442C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1785C>T
  hgvsp: ENST00000545957.1:c.1785C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7902
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8837
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile954Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/6-131917249-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917249
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917250
    reference: chr 6
allele count: 3
allele frequency: 2.472065658063878e-5
allele num: 121356
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2850dupT
  hgvsp: ENSP00000357037.1:p.Val951CysfsTer24
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2832dupT
  hgvsp: ENSP00000357047.3:p.Val945CysfsTer24
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.412dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2832dupT
  hgvsp: ENSP00000357039.3:p.Val945CysfsTer24
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2850dupT
  hgvsp: ENSP00000346588.4:p.Val951CysfsTer24
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2850dupT
  hgvsp: ENSP00000384536.3:p.Val951CysfsTer24
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1755dupT
  hgvsp: ENSP00000439977.1:p.Val586CysfsTer24
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val945CysfsTer24
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

6-131917268-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917268
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917268
    reference: chr 6
allele count: 276
allele frequency: 2.276063399910936e-3
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2832G>A
  hgvsp: ENST00000368058.1:c.2832G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2832G>A
  hgvsp: ENST00000354577.4:c.2832G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2832G>A
  hgvsp: ENST00000403834.3:c.2832G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1737G>A
  hgvsp: ENST00000545957.1:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.394G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2814G>A
  hgvsp: ENST00000368060.3:c.2814G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2814G>A
  hgvsp: ENST00000368068.3:c.2814G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 9.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 20829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala938Ala
num of homozygotes: 1
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

6-131917269-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917269
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917269
    reference: chr 6
allele count: 2
allele frequency: 1.649756660892518e-5
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.393C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1736C>T
  hgvsp: ENSP00000439977.1:p.Ala579Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2813C>T
  hgvsp: ENSP00000357039.3:p.Ala938Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2831C>T
  hgvsp: ENSP00000357037.1:p.Ala944Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2813C>T
  hgvsp: ENSP00000357047.3:p.Ala938Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2831C>T
  hgvsp: ENSP00000346588.4:p.Ala944Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2831C>T
  hgvsp: ENSP00000384536.3:p.Ala944Val
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36396
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala938Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

6-131917270-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917270
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917270
    reference: chr 6
allele count: 2
allele frequency: 1.649892756970797e-5
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.392G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1735G>A
  hgvsp: ENSP00000439977.1:p.Ala579Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2812G>A
  hgvsp: ENSP00000357047.3:p.Ala938Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2830G>A
  hgvsp: ENSP00000357037.1:p.Ala944Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2830G>A
  hgvsp: ENSP00000346588.4:p.Ala944Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2812G>A
  hgvsp: ENSP00000357039.3:p.Ala938Thr
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2830G>A
  hgvsp: ENSP00000384536.3:p.Ala944Thr
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20913
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7886
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala938Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ

6-131917271-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917271
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917271
    reference: chr 6
allele count: 12
allele frequency: 9.899846552378439e-5
allele num: 121214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.391C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2829C>T
  hgvsp: ENST00000354577.4:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2811C>T
  hgvsp: ENST00000368068.3:c.2811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2829C>T
  hgvsp: ENST00000368058.1:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2811C>T
  hgvsp: ENST00000368060.3:c.2811C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1734C>T
  hgvsp: ENST00000545957.1:c.1734C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2829C>T
  hgvsp: ENST00000403834.3:c.2829C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8811
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 7885
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36364
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu937Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-131917274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917274
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917274
    reference: chr 6
allele count: 2
allele frequency: 1.650219479190732e-5
allele num: 121196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.388C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2826C>T
  hgvsp: ENST00000403834.3:c.2826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2808C>T
  hgvsp: ENST00000368068.3:c.2808C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2826C>T
  hgvsp: ENST00000368058.1:c.2826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2826C>T
  hgvsp: ENST00000354577.4:c.2826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2808C>T
  hgvsp: ENST00000368060.3:c.2808C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1731C>T
  hgvsp: ENST00000545957.1:c.1731C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7888
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2007
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8801
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly936Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

6-131917288-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917288
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917288
    reference: chr 6
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2794T>C
  hgvsp: ENST00000368068.3:c.2794T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2812T>C
  hgvsp: ENST00000354577.4:c.2812T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2812T>C
  hgvsp: ENST00000403834.3:c.2812T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2794T>C
  hgvsp: ENST00000368060.3:c.2794T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2812T>C
  hgvsp: ENST00000368058.1:c.2812T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1717T>C
  hgvsp: ENST00000545957.1:c.1717T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.374T>C
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36169
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8800
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1497
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu932Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

6-131917288-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917288
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917288
    reference: chr 6
allele count: 1
allele frequency: 8.261731658955718e-6
allele num: 121040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.374T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2812T>A
  hgvsp: ENSP00000384536.3:p.Leu938Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2794T>A
  hgvsp: ENSP00000357047.3:p.Leu932Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2812T>A
  hgvsp: ENSP00000346588.4:p.Leu938Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2812T>A
  hgvsp: ENSP00000357037.1:p.Leu938Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2794T>A
  hgvsp: ENSP00000357039.3:p.Leu932Met
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1717T>A
  hgvsp: ENSP00000439977.1:p.Leu573Met
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8800
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu932Met
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

6-131917301-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917301
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917301
    reference: chr 6
allele count: 2
allele frequency: 1.65508109897385e-5
allele num: 120840
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2781A>G
  hgvsp: ENST00000368068.3:c.2781A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.361A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2781A>G
  hgvsp: ENST00000368060.3:c.2781A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2799A>G
  hgvsp: ENST00000368058.1:c.2799A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2799A>G
  hgvsp: ENST00000354577.4:c.2799A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1704A>G
  hgvsp: ENST00000545957.1:c.1704A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2799A>G
  hgvsp: ENST00000403834.3:c.2799A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 7.75e1
  variant carriers: 0
hgvs: c.2781A>G
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

6-131917308-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917308
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917308
    reference: chr 6
allele count: 2
allele frequency: 1.657797450307521e-5
allele num: 120642
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-5C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-5C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-5C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-5C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-5C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-5C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.354C>T
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35622
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8797
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2779-5C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP

6-131917312-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917312
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917312
    reference: chr 6
allele count: 1
allele frequency: 8.298755186721992e-6
allele num: 120500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-9A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-9A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-9A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.350A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-9A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-9A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-9A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8795
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/6-131917315-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917315
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917315
    reference: chr 6
allele count: 1
allele frequency: 8.318913882603488e-6
allele num: 120208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-12T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-12T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-12T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.347T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-12T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-12T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-12T>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7759
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

6-131917316-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917316
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917316
    reference: chr 6
allele count: 1
allele frequency: 8.31849867735871e-6
allele num: 120214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-13C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-13C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-13C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-13C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-13C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.346C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-13C>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20698
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7758
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34854
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8794
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

6-131917319-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917319
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917319
    reference: chr 6
allele count: 9
allele frequency: 7.513148009015778e-5
allele num: 119790
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-16C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-16C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-16C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-16C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.343C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-16C>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-16C>T
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20490
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8797
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1897
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

6-131917321-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917321
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917321
    reference: chr 6
allele count: 3
allele frequency: 2.509788173878125e-5
allele num: 119532
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-18A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-18A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-18A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-18A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-18A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-18A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.341A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14858
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2329
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2282
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7594
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8793
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 33280
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

6-131917326-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917326
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917326
    reference: chr 6
allele count: 1
allele frequency: 8.406752303450132e-6
allele num: 118952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-23T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-23T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.336T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-23T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-23T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-23T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-23T>A
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7350
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8791
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1481
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2316
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

6-131917338-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917338
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917339
    reference: chr 6
allele count: 4
allele frequency: 3.412037668895865e-5
allele num: 117232
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-36dupA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-36dupA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-36dupA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-36dupA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-36dupA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.323dupA
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-36dupA
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9606
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6446
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 854
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2213
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

6-131917341-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917341
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917341
    reference: chr 6
allele count: 1
allele frequency: 8.569861511037982e-6
allele num: 116688
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-38A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-38A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-38A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-38A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.321A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-38A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-38A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9031
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5067
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8786
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ

6-131917344-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917344
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917344
    reference: chr 6
allele count: 10
allele frequency: 8.615936035290874e-5
allele num: 116064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-41A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.318A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-41A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-41A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-41A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-41A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-41A>T
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9424
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13159
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2270
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4965
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8801
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 4491
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

6-131917344-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917344
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917345
    reference: chr 6
allele count: 1
allele frequency: 8.615936035290874e-6
allele num: 116064
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.317dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-42dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-42dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-42dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-42dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-42dupT
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-42dupT
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5263
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

6-131917345-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917345
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917345
    reference: chr 6
allele count: 70
allele frequency: 6.022956066837604e-4
allele num: 116222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-42T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.317T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-42T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-42T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-42T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-42T>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-42T>A
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10601
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9430
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 13192
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6934
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17485
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4511
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-131917350-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917350
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917350
    reference: chr 6
allele count: 1
allele frequency: 8.712471031033823e-6
allele num: 114778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-47T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.312T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-47T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-47T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-47T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-47T>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-47T>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13059
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5445
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4035
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11826
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8781
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4836
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/6-131917353-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917353
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917353
    reference: chr 6
allele count: 9
allele frequency: 7.88684999211315e-5
allele num: 114114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-50G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.309G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-50G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-50G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-50G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-50G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-50G>T
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10442
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10443
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3035
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2022
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4102
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5511
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10215
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

6-131917354-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917354
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917354
    reference: chr 6
allele count: 1
allele frequency: 8.757794437048973e-6
allele num: 114184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2797-51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2779-51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.308A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1702-51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2779-51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2797-51A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2797-51A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10409
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1068
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3998
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3960
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1473
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4859
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3043
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5525
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

6-131917613-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917613
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917613
    reference: chr 6
allele count: 2
allele frequency: 1.648206751054852e-5
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2796+45A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2778+45A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2796+45A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2796+45A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1701+45A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.49A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2778+45A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8023
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

6-131917627-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917627
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917627
    reference: chr 6
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2778+31C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1701+31C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.35C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2796+31C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2796+31C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2796+31C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2778+31C>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28623
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37501
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8497
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

6-131917631-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917631
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917631
    reference: chr 6
allele count: 7
allele frequency: 5.767772980455489e-5
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1701+27T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2796+27T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2796+27T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.31T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2796+27T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2778+27T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2778+27T>C
  variant of: http://identifiers.org/hgnc/2372
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: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37532
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum

6-131917632-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917632
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917632
    reference: chr 6
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2796+26A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1701+26A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2796+26A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2796+26A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.30A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2778+26A>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2778+26A>G
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8011
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-131917634-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917634
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917634
    reference: chr 6
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1701+24A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2778+24A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.28A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2796+24A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2778+24A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2796+24A>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2796+24A>T
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11492
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8010
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-131917642-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917642
    reference: chr 6
allele count: 38
allele frequency: 3.130818791503947e-4
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2796+16G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2778+16G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.20G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2796+16G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2796+16G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2778+16G>T
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1701+16G>T
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28628
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8107
  bin: 9.75e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2113
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP

6-131917642-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917642
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917642
    reference: chr 6
allele count: 425
allele frequency: 3.501573648392572e-3
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2778+16G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2796+16G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2796+16G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1701+16G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2796+16G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.20G>A
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2778+16G>A
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 9389
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28628
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 9.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 9.75e1
  variant carriers: 176
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 7.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8107
  bin: 9.75e1
  variant carriers: 418
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 7
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

6-131917644-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917644
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917644
    reference: chr 6
allele count: 7
allele frequency: 5.767297773823059e-5
allele num: 121374
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2778+14T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1701+14T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2796+14T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2796+14T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.18T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2796+14T>C
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2778+14T>C
  variant of: http://identifiers.org/hgnc/2372
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8576
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2132
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

6-131917661-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917661
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917661
    reference: chr 6
allele count: 2
allele frequency: 1.647582173160887e-5
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1698C>G
  hgvsp: ENSP00000439977.1:p.His566Gln
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2775C>G
  hgvsp: ENSP00000357039.3:p.His925Gln
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112282
  ensembl transcript: ENST00000479213
  gene symbol: MED23
  hgvsc: ENST00000479213.1:n.1C>G
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2793C>G
  hgvsp: ENSP00000384536.3:p.His931Gln
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2793C>G
  hgvsp: ENSP00000346588.4:p.His931Gln
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2775C>G
  hgvsp: ENSP00000357047.3:p.His925Gln
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2793C>G
  hgvsp: ENSP00000357037.1:p.His931Gln
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9459
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37892
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8580
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.His925Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS

6-131917668-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917668
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917668
    reference: chr 6
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2786A>T
  hgvsp: ENSP00000357037.1:p.Asn929Ile
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2786A>T
  hgvsp: ENSP00000384536.3:p.Asn929Ile
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2768A>T
  hgvsp: ENSP00000357047.3:p.Asn923Ile
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2786A>T
  hgvsp: ENSP00000346588.4:p.Asn929Ile
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1691A>T
  hgvsp: ENSP00000439977.1:p.Asn564Ile
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2768A>T
  hgvsp: ENSP00000357039.3:p.Asn923Ile
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8579
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37894
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn923Ile
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

6-131917672-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917672
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917672
    reference: chr 6
allele count: 3
allele frequency: 2.471291826614165e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2782A>G
  hgvsp: ENSP00000384536.3:p.Met928Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2764A>G
  hgvsp: ENSP00000357047.3:p.Met922Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1687A>G
  hgvsp: ENSP00000439977.1:p.Met563Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2782A>G
  hgvsp: ENSP00000346588.4:p.Met928Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2764A>G
  hgvsp: ENSP00000357039.3:p.Met922Val
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2782A>G
  hgvsp: ENSP00000357037.1:p.Met928Val
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11549
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28867
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7686
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Met922Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

6-131917673-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131917673
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131917673
    reference: chr 6
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357039
  ensembl transcript: ENST00000368060
  gene symbol: MED23
  hgvsc: ENST00000368060.3:c.2763C>T
  hgvsp: ENST00000368060.3:c.2763C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000384536
  ensembl transcript: ENST00000403834
  gene symbol: MED23
  hgvsc: ENST00000403834.3:c.2781C>T
  hgvsp: ENST00000403834.3:c.2781C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000439977
  ensembl transcript: ENST00000545957
  gene symbol: MED23
  hgvsc: ENST00000545957.1:c.1686C>T
  hgvsp: ENST00000545957.1:c.1686C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357037
  ensembl transcript: ENST00000368058
  gene symbol: MED23
  hgvsc: ENST00000368058.1:c.2781C>T
  hgvsp: ENST00000368058.1:c.2781C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000346588
  ensembl transcript: ENST00000354577
  gene symbol: MED23
  hgvsc: ENST00000354577.4:c.2781C>T
  hgvsp: ENST00000354577.4:c.2781C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112282
  ensembl protein: ENSP00000357047
  ensembl transcript: ENST00000368068
  gene symbol: MED23
  hgvsc: ENST00000368068.3:c.2763C>T
  hgvsp: ENST00000368068.3:c.2763C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/2372
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9453
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His921His
num of homozygotes: 0
reference allele: G

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

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

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

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

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3312
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3270
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8813
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1942
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66344
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.42e0

DP
type: SiteQuality
SIO_000300: 2.419951e6

QD
type: SiteQuality
SIO_000300: 1.137e1

VQSLOD
type: SiteQuality
SIO_000300: 4.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

FS
type: SiteQuality
SIO_000300: 2.917e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.27e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.763718023823472e-5
allele num: 10242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66284
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

MQ
type: SiteQuality
SIO_000300: 5.74e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

QD
type: SiteQuality
SIO_000300: 1.1e1

VQSLOD
type: SiteQuality
SIO_000300: 4.02e0

DP
type: SiteQuality
SIO_000300: 2.418338e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.422e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

GenotypeQuality
all individuals: 1040
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8309
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
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: 902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 2.408721e6

FS
type: SiteQuality
SIO_000300: 1.797e0

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

QD
type: SiteQuality
SIO_000300: 1.384e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8133
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2018
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.994813484939158e-4
allele num: 10026
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.731002250302925e-4
allele num: 11554
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.222e1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

DP
type: SiteQuality
SIO_000300: 2.402788e6

FS
type: SiteQuality
SIO_000300: 1.162e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
all individuals: 33663
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7915
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 2018
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.045901739209893e-5
allele num: 65662
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.398558e6

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.68e0

FS
type: SiteQuality
SIO_000300: 1.998e0

QD
type: SiteQuality
SIO_000300: 1.455e1

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1901
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3108
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 2018
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3295
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3424
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 7836
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523879186858066e-5
allele num: 65622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.004217714400482e-4
allele num: 9958
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

FS
type: SiteQuality
SIO_000300: 7.395e0

DP
type: SiteQuality
SIO_000300: 2.397163e6

VQSLOD
type: SiteQuality
SIO_000300: 3.36e-1

QD
type: SiteQuality
SIO_000300: 1.325e1

MQRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 49
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 1891
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variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65424
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9834
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.29e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

FS
type: SiteQuality
SIO_000300: 1.1679e1

DP
type: SiteQuality
SIO_000300: 2.392982e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 3265
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65344
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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African
type: Population
allele count: 1
allele frequency: 1.019160211985324e-4
allele num: 9812
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.206e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.391341e6

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

QD
type: SiteQuality
SIO_000300: 1.51e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.688e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 253
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.068425897514575e-5
allele num: 65180
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

FS
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.161e1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 5.979e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.133e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 85
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.328830926874709e-4
allele num: 8588
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.909e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.92e-1

QD
type: SiteQuality
SIO_000300: 1.13e1

DP
type: SiteQuality
SIO_000300: 2.384387e6

GenotypeQuality
all individuals: 121
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3264
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 533
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 257
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GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 6911
bin: 6.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 5
allele frequency: 3.032140691328078e-4
allele num: 16490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64956
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.296e0

DP
type: SiteQuality
SIO_000300: 2.382346e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.893e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.5e-2

QD
type: SiteQuality
SIO_000300: 1.273e1

GenotypeQuality
all individuals: 3290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33666
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 263
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 3.187420314492138e-4
allele num: 9412
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64584
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

QD
type: SiteQuality
SIO_000300: 2.311e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.948e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.375741e6

GenotypeQuality
all individuals: 1847
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551253412757508e-5
allele num: 64464
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.19e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.296e0

QD
type: SiteQuality
SIO_000300: 1.351e1

DP
type: SiteQuality
SIO_000300: 2.375639e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.61e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 722
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2099
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8956
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2347
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 925
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variant carriers: 0

GenotypeQuality
all individuals: 1697
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64002
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.085540599218411e-4
allele num: 9212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6562
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: 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: 16420
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.159e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
SIO_000300: 1.544e1

DP
type: SiteQuality
SIO_000300: 1.832224e6

GenotypeQuality
all individuals: 971
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1528
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1960
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variant carriers: 0

GenotypeQuality
all individuals: 8926
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.11779011036977e-5
allele num: 64148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8114
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.369e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

VQSLOD
type: SiteQuality
SIO_000300: -4.296e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

QD
type: SiteQuality
SIO_000300: 1.423e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 1.86445e6

GenotypeQuality
all individuals: 888
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8926
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30660
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64180
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.082251082251082e-4
allele num: 9240
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.805e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

DP
type: SiteQuality
SIO_000300: 1.867262e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.166e0

QD
type: SiteQuality
SIO_000300: 8.710000000000001e0

GenotypeQuality
all individuals: 137
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
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GenotypeQuality
all individuals: 445
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
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variant carriers: 0

GenotypeQuality
all individuals: 484
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variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 1956
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variant carriers: 0

GenotypeQuality
all individuals: 8920
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variant carriers: 1

GenotypeQuality
all individuals: 884
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550916591705698e-5
allele num: 64478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.764e0

DP
type: SiteQuality
SIO_000300: 1.888582e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.273e1

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

MQRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.97e-1

GenotypeQuality
all individuals: 8920
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 7524
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 178
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GenotypeQuality
all individuals: 619
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 445
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variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11396
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
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)
type: Population
allele count: 2
allele frequency: 3.101833183411396e-5
allele num: 64478
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.223690651003426e-4
allele num: 8172
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.764e0

QD
type: SiteQuality
SIO_000300: 1.273e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.97e-1

DP
type: SiteQuality
SIO_000300: 1.888582e6

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 32658
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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
all individuals: 7517
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GenotypeQuality
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GenotypeQuality
all individuals: 172
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variant carriers: 0

GenotypeQuality
all individuals: 9170
bin: 9.75e1
variant carriers: 390

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.2278547623224e-3
allele num: 11402
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.141552511415525e-3
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.295120061967467e-5
allele num: 64550
num of homozygotes: 0

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

African
type: Population
allele count: 380
allele frequency: 4.086900408690041e-2
allele num: 9298
num of homozygotes: 7

South Asian
type: Population
allele count: 2
allele frequency: 1.216693028348948e-4
allele num: 16438
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.898182e6

VQSLOD
type: SiteQuality
SIO_000300: 6.6e0

MQRankSum
type: SiteQuality
SIO_000300: 2.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.456e1

GenotypeQuality
all individuals: 333
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variant carriers: 0

GenotypeQuality
all individuals: 375
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GenotypeQuality
all individuals: 264
bin: 3.75e1
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GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 2350
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7643
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GenotypeQuality
all individuals: 1497
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.758101243650377e-5
allele num: 11418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8236
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 880
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.019e0

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.072e1

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
all individuals: 257
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GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 866
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GenotypeQuality
all individuals: 1975
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variant carriers: 0

GenotypeQuality
all individuals: 8836
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2359
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.203759077317386e-4
allele num: 9364
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

FS
type: SiteQuality
SIO_000300: 5.659e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 1.906143e6

VQSLOD
type: SiteQuality
SIO_000300: 4.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

QD
type: SiteQuality
SIO_000300: 1.636e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 835
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520727516043675e-5
allele num: 65758
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e0

FS
type: SiteQuality
SIO_000300: 1.314e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.923545e6

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.704e1

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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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variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
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: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9634
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65842
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.03e0

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

FS
type: SiteQuality
SIO_000300: 2.876e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.4e-1

DP
type: SiteQuality
SIO_000300: 1.92533e6

MQ
type: SiteQuality
SIO_000300: 5.987e1

QD
type: SiteQuality
SIO_000300: 1.234e1

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

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1515
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35535
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variant carriers: 0

GenotypeQuality
all individuals: 1986
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.038590094196293e-4
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.92916e6

QD
type: SiteQuality
SIO_000300: 1.064e1

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.029e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.8e-2

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

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

GenotypeQuality
all individuals: 1985
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
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GenotypeQuality
all individuals: 7820
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GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 2381
bin: 7.75e1
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8849
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.613695765812859e-4
allele num: 11478
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.232142857142857e-3
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.568418503269556e-5
allele num: 66064
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.645e0

DP
type: SiteQuality
SIO_000300: 1.92989e6

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 8839
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 617
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66196
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.179523472517103e-4
allele num: 8478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.386e1

VQSLOD
type: SiteQuality
SIO_000300: -1.306e0

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

FS
type: SiteQuality
SIO_000300: 2.958e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.26e-1

MQ
type: SiteQuality
SIO_000300: 5.775e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.522e0

DP
type: SiteQuality
SIO_000300: 1.932035e6

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

GenotypeQuality
all individuals: 2384
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 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: 11528
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 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: 3
allele frequency: 4.509379509379509e-5
allele num: 66528
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.213444970270598e-4
allele num: 16482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e-1

DP
type: SiteQuality
SIO_000300: 1.940407e6

VQSLOD
type: SiteQuality
SIO_000300: 8.45e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

FS
type: SiteQuality
SIO_000300: 5.52e-1

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 241
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variant carriers: 0

GenotypeQuality
all individuals: 7882
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GenotypeQuality
all individuals: 8840
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004627125773691e-5
allele num: 66564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.83e0

FS
type: SiteQuality
SIO_000300: 1.159e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.941728e6

QD
type: SiteQuality
SIO_000300: 1.402e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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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: 1

GenotypeQuality
all individuals: 2013
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variant carriers: 0

GenotypeQuality
all individuals: 7886
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

DP
type: SiteQuality
SIO_000300: 1.943461e6

FS
type: SiteQuality
SIO_000300: 4.43e-1

QD
type: SiteQuality
SIO_000300: 1.108e1

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.337e0

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

MQRankSum
type: SiteQuality
SIO_000300: 4.37e-1

GenotypeQuality
all individuals: 131
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2385
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GenotypeQuality
all individuals: 876
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 7886
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variant carriers: 0

GenotypeQuality
all individuals: 618
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variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
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: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.322e0

ReadPosRankSum
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SIO_000300: -3.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.51e0

DP
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SIO_000300: 1.944218e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.99e-1

QD
type: SiteQuality
SIO_000300: 1.474e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11574
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)
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allele count: 2
allele frequency: 3.000930288389401e-5
allele num: 66646
num of homozygotes: 0

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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num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.941e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.21e0

BaseQRankSum
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SIO_000300: 6.79e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.89e-1

DP
type: SiteQuality
SIO_000300: 1.944372e6

MQRankSum
type: SiteQuality
SIO_000300: 9.68e-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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variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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InbreedingCoeff
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ClippingRankSum
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QD
type: SiteQuality
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MQRankSum
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MQ
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BaseQRankSum
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.01e0

FS
type: SiteQuality
SIO_000300: 1.18e0

DP
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SIO_000300: 1.944996e6

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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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.945135e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.865e0

FS
type: SiteQuality
SIO_000300: 2.576e0

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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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variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 66722
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.635767970707265e-5
allele num: 10378
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.034e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.078e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

DP
type: SiteQuality
SIO_000300: 1.946133e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.64e-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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

FS
type: SiteQuality
SIO_000300: 2.448e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.53e-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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variant carriers: 0

European (Finnish)
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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: 10384
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: 66724
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele num: 16512
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BaseQRankSum
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QD
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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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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variant carriers: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66718
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
type: Population
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African
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South Asian
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Latino
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East Asian
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
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ReadPosRankSum
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DP
type: SiteQuality
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InbreedingCoeff
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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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variant carriers: 275

East Asian
type: Population
allele count: 0
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African
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Latino
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allele frequency: 9.502418797512094e-4
allele num: 11576
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European (Finnish)
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allele count: 41
allele frequency: 6.198971877834896e-3
allele num: 6614
num of homozygotes: 0

Other
type: Population
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allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
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allele count: 168
allele frequency: 2.519420533277346e-3
allele num: 66682
num of homozygotes: 0

South Asian
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allele frequency: 3.270348837209302e-3
allele num: 16512
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DP
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QD
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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MQ
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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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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

Other
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East Asian
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allele num: 8640
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African
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European (Finnish)
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Latino
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South Asian
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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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: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 9.12e-1

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.75e0

DP
type: SiteQuality
SIO_000300: 1.944719e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.65e-1

FS
type: SiteQuality
SIO_000300: 5.2e0

QD
type: SiteQuality
SIO_000300: 1.276e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
all individuals: 2008
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 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: 906
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 0

Latino
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allele count: 10
allele frequency: 8.641548565502938e-4
allele num: 11572
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.885e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
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ReadPosRankSum
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SIO_000300: -1.8e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.945333e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.39e-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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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: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.314279102059708e-4
allele num: 8642
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.22e-1

QD
type: SiteQuality
SIO_000300: 1.051e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.324e0

MQRankSum
type: SiteQuality
SIO_000300: 9.21e-1

FS
type: SiteQuality
SIO_000300: 9.541e0

DP
type: SiteQuality
SIO_000300: 1.94433e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.29e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2009
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

FS
type: SiteQuality
SIO_000300: 5.029e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.94e-1

DP
type: SiteQuality
SIO_000300: 1.941749e6

QD
type: SiteQuality
SIO_000300: 1.365e1

MQRankSum
type: SiteQuality
SIO_000300: 8.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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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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
all individuals: 863
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.941749e6

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.365e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.96e0

FS
type: SiteQuality
SIO_000300: 5.029e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.94e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
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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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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
all individuals: 8800
bin: 9.75e1
variant carriers: 2

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005981903988938e-5
allele num: 66534
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.938658e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.25e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

FS
type: SiteQuality
SIO_000300: 4.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.286e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.793e1

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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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010325416177489e-5
allele num: 66438
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.722e0

MQ
type: SiteQuality
SIO_000300: 5.912e1

VQSLOD
type: SiteQuality
SIO_000300: -4.777e-1

DP
type: SiteQuality
SIO_000300: 1.934775e6

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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bin: 7.5e0
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.93081e6

GenotypeQuality
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bin: 8.25e1
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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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510984859931704e-5
allele num: 66182
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9980
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East Asian
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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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
all individuals: 18
bin: 4.25e1
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GenotypeQuality
all individuals: 176
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510984859931704e-5
allele num: 66182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.022e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.06e0

VQSLOD
type: SiteQuality
SIO_000300: -1.139e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

DP
type: SiteQuality
SIO_000300: 1.92458e6

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.862e1

GenotypeQuality
all individuals: 2334
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7655
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.064833065469873e-5
allele num: 65954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.582650894752805e-4
allele num: 6594
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.914196e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.872e0

VQSLOD
type: SiteQuality
SIO_000300: 5.68e0

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.83e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.457e1

GenotypeQuality
all individuals: 1951
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8476
num of homozygotes: 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: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.5584391904212e-5
allele num: 65812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.36e-1

DP
type: SiteQuality
SIO_000300: 1.905671e6

FS
type: SiteQuality
SIO_000300: 5.668e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 9.67e0

GenotypeQuality
all individuals: 95
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3351
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
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: 1
allele frequency: 1.527230520174715e-5
allele num: 65478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.938e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.52e-1

QD
type: SiteQuality
SIO_000300: 1.375e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.933e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

DP
type: SiteQuality
SIO_000300: 1.879779e6

GenotypeQuality
all individuals: 3444
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22174
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8795
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5103
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6105
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.553760099440646e-5
allele num: 64360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16352
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.682789098944267e-4
allele num: 8146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

FS
type: SiteQuality
SIO_000300: 6.661e0

DP
type: SiteQuality
SIO_000300: 1.770018e6

QD
type: SiteQuality
SIO_000300: 2.098e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

GenotypeQuality
all individuals: 3666
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5560
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2197
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2207
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 850
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11276
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9586
num of homozygotes: 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: 6532
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.128953174797744e-5
allele num: 16316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8060
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 1.698e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.536e0

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-2

DP
type: SiteQuality
SIO_000300: 1.738081e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 315
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2012
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5263
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.531862745098039e-4
allele num: 6528
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.43040362127499e-5
allele num: 63624
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.148548942449582e-5
allele num: 16264
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.095118374188141e-4
allele num: 9546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8000
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

FS
type: SiteQuality
SIO_000300: 2.059e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

DP
type: SiteQuality
SIO_000300: 1.72193e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

QD
type: SiteQuality
SIO_000300: 1.132e1

GenotypeQuality
all individuals: 2270
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8801
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4491
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.571733936879165e-5
allele num: 63624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8000
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

FS
type: SiteQuality
SIO_000300: 2.059e0

DP
type: SiteQuality
SIO_000300: 1.72193e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

QD
type: SiteQuality
SIO_000300: 1.132e1

GenotypeQuality
all individuals: 1652
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4994
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 8834
bin: 9.75e1
variant carriers: 67

GenotypeQuality
all individuals: 2274
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 837
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GenotypeQuality
all individuals: 283
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5305
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1441
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.139388865634157e-4
allele num: 9556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.532332209623046e-4
allele num: 6526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11234
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.597396217145664e-4
allele num: 16284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 52
allele frequency: 8.160446941401714e-4
allele num: 63722
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

DP
type: SiteQuality
SIO_000300: 1.721364e6

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.19e-1

FS
type: SiteQuality
SIO_000300: 3.281e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.55e-1

GenotypeQuality
all individuals: 1485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4366
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2299
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variant carriers: 0

GenotypeQuality
all individuals: 937
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GenotypeQuality
all individuals: 2176
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variant carriers: 0

GenotypeQuality
all individuals: 844
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4508
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 598
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2046
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7866
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.169031462060457e-5
allele num: 16210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62734
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.136e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.1e0

MQRankSum
type: SiteQuality
SIO_000300: -2.15e-1

QD
type: SiteQuality
SIO_000300: 1.485e1

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.669999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.692039e6

GenotypeQuality
all individuals: 3943
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5191
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4830
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 7.5e0
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GenotypeQuality
all individuals: 8787
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 842
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3025
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 6.423432682425488e-5
allele num: 62272
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African
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allele frequency: 1.056412423410099e-4
allele num: 9466
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.809954751131222e-4
allele num: 11050
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Other
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QD
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MQ
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DP
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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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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Other
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European (Non-Finnish)
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allele frequency: 1.604827320580306e-5
allele num: 62312
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ReadPosRankSum
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MQRankSum
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DP
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MQ
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FS
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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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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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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allele num: 66714
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Other
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Latino
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South Asian
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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BaseQRankSum
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FS
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MQRankSum
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InbreedingCoeff
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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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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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South Asian
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MQRankSum
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FS
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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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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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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allele frequency: 4.240368306275745e-4
allele num: 16508
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African
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European (Non-Finnish)
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num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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MQ
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VQSLOD
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FS
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QD
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ReadPosRankSum
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SIO_000300: 9.330000000000001e-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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Latino
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allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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African
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allele num: 10400
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European (Finnish)
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South Asian
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QD
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DP
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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MQRankSum
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 6612
num of homozygotes: 0

South Asian
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Latino
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African
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East Asian
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Other
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European (Non-Finnish)
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VQSLOD
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QD
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ClippingRankSum
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MQ
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DP
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BaseQRankSum
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MQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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allele frequency: 4.395095998149434e-3
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European (Non-Finnish)
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Latino
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Other
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South Asian
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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VQSLOD
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QD
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MQ
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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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European (Finnish)
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Latino
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Other
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African
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East Asian
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South Asian
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European (Non-Finnish)
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allele frequency: 8.992266650680415e-5
allele num: 66724
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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Latino
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South Asian
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East Asian
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European (Finnish)
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African
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Other
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InbreedingCoeff
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FS
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MQ
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 497
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7689
bin: 9.75e1
variant carriers: 2

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: 11576
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.954699e6

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

QD
type: SiteQuality
SIO_000300: 1.147e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.9e-1

FS
type: SiteQuality
SIO_000300: 1.614e0

GenotypeQuality
all individuals: 2133
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7687
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 497
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
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: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

DP
type: SiteQuality
SIO_000300: 1.954766e6

VQSLOD
type: SiteQuality
SIO_000300: -3.389e-1

FS
type: SiteQuality
SIO_000300: 6.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.187e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.412e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.17e-1

MQ
type: SiteQuality
SIO_000300: 5.897e1

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37898
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8576
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.86e0

FS
type: SiteQuality
SIO_000300: 4.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 1.954883e6

VQSLOD
type: SiteQuality
SIO_000300: 6.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.47e0

QD
type: SiteQuality
SIO_000300: 1.396e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3