7-5434204-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434204
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434204
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 20868
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.210T>C
  hgvsp: ENST00000430969.1:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.210T>C
  hgvsp: ENST00000399537.4:c.210T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-13T>C
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-13T>C
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32334
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31228
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3404
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe70Phe
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD

7-5434220-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434220
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434220
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 20106
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-29C>G
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.194C>G
  hgvsp: ENSP00000395538.1:p.Ala65Gly
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-29C>G
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.194C>G
  hgvsp: ENSP00000382452.4:p.Ala65Gly
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8571
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32475
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3047
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala65Gly
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

7-5434220-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434220
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434220
    reference: chr 7
allele count: 2
allele frequency: 9.947279419078882e-5
allele num: 20106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.194C>A
  hgvsp: ENSP00000382452.4:p.Ala65Asp
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.194C>A
  hgvsp: ENSP00000395538.1:p.Ala65Asp
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-29C>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-29C>A
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32475
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8571
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala65Asp
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

7-5434234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434234
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434234
    reference: chr 7
allele count: 1
allele frequency: 5.136106831022085e-5
allele num: 19470
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.188-8C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-35-8C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.188-8C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-35-8C>T
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33444
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
hgvs: c.188-8C>T
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

7-5434234-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434234
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434234
    reference: chr 7
allele count: 10
allele frequency: 5.136106831022085e-4
allele num: 19470
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-35-8C>G
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-35-8C>G
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.188-8C>G
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.188-8C>G
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34496
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3076
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33444
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
hgvs: c.188-8C>G
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD

7-5434244-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434244
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434244
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 18978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.188-18C>G
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-35-18C>G
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.188-18C>G
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-35-18C>G
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4853
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33262
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

7-5434249-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434249
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434249
    reference: chr 7
allele count: 2
allele frequency: 1.07515320933233e-4
allele num: 18602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-35-23G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.188-23G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.188-23G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-35-23G>A
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33788
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3060
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2265
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2966
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31817
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

7-5434265-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434265
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434265
    reference: chr 7
allele count: 1
allele frequency: 5.869233478107759e-5
allele num: 17038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.188-39G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-35-39G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.188-39G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-35-39G>A
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29502
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 441
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1140
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

7-5434274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5434274
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5434274
    reference: chr 7
allele count: 1
allele frequency: 6.377551020408164e-5
allele num: 15680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000410856
  ensembl transcript: ENST00000434361
  gene symbol: TNRC18
  hgvsc: ENST00000434361.1:c.-35-48C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-35-48C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.188-48C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.188-48C>T
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1337
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16511
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13179
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3062
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

7-5459920-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5459920
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5459920
    reference: chr 7
allele count: 254
allele frequency: 3.898096992019644e-2
allele num: 6516
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.187+771G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188365
  ensembl transcript: ENST00000455866
  gene symbol: AC092171.2
  hgvsc: ENST00000455866.1:n.423+21C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241269
  ensembl transcript: ENST00000342963
  gene symbol: AC093620.5
  hgvsc: ENST00000342963.2:n.152-47C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.187+771G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-36+5002G>A
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 7.5e0
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 5888
  bin: 2.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 1.25e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 8.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 2.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 6.75e1
  variant carriers: 3
num of homozygotes: 7
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

7-5459924-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5459924
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5459924
    reference: chr 7
allele count: 0
allele frequency: 0.0e0
allele num: 6656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-36+4998C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188365
  ensembl transcript: ENST00000455866
  gene symbol: AC092171.2
  hgvsc: ENST00000455866.1:n.423+25G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.187+767C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241269
  ensembl transcript: ENST00000342963
  gene symbol: AC093620.5
  hgvsc: ENST00000342963.2:n.152-43G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.187+767C>T
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4049
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1760
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-10603505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603505
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603505
    reference: chr 11
allele count: 2
allele frequency: 1.656836105772417e-5
allele num: 120712
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1324G>A
  hgvsp: ENSP00000433296.2:p.Glu442Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2242G>A
  hgvsp: ENSP00000414598.1:p.Glu748Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1996G>A
  hgvsp: ENSP00000446764.1:p.Glu666Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-4069C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1996G>A
  hgvsp: ENSP00000448278.1:p.Glu666Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1324G>A
  hgvsp: ENSP00000401205.1:p.Glu442Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1651G>A
  hgvsp: ENSP00000437784.1:p.Glu551Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1794G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2245G>A
  hgvsp: ENSP00000432436.1:p.Glu749Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2269G>A
  hgvsp: ENSP00000412130.2:p.Glu757Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1996G>A
  hgvsp: ENSP00000432067.2:p.Glu666Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1324G>A
  hgvsp: ENSP00000441971.1:p.Glu442Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*161G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1324G>A
  hgvsp: ENSP00000453013.1:p.Glu442Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12159C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2188G>A
  hgvsp: ENSP00000412229.1:p.Glu730Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17728G>A
  variant of: http://identifiers.org/hgnc/14687
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu757Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

11-10603528-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603528
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603528
    reference: chr 11
allele count: 75
allele frequency: 6.219936971305357e-4
allele num: 120580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-4046T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2246A>G
  hgvsp: ENSP00000412130.2:p.Lys749Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1973A>G
  hgvsp: ENSP00000448278.1:p.Lys658Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2222A>G
  hgvsp: ENSP00000432436.1:p.Lys741Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2219A>G
  hgvsp: ENSP00000414598.1:p.Lys740Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17751A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1301A>G
  hgvsp: ENSP00000401205.1:p.Lys434Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1301A>G
  hgvsp: ENSP00000453013.1:p.Lys434Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2165A>G
  hgvsp: ENSP00000412229.1:p.Lys722Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1771A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1301A>G
  hgvsp: ENSP00000441971.1:p.Lys434Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1973A>G
  hgvsp: ENSP00000446764.1:p.Lys658Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1973A>G
  hgvsp: ENSP00000432067.2:p.Lys658Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*138A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1301A>G
  hgvsp: ENSP00000433296.2:p.Lys434Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12136T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1628A>G
  hgvsp: ENSP00000437784.1:p.Lys543Arg
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 12268
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys749Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

11-10603533-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603533
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603533
    reference: chr 11
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214T>C
  hgvsp: ENST00000421747.1:c.2214T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217T>C
  hgvsp: ENST00000531107.1:c.2217T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160T>C
  hgvsp: ENST00000436272.1:c.2160T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296T>C
  hgvsp: ENST00000534266.2:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968T>C
  hgvsp: ENST00000547195.1:c.1968T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623T>C
  hgvsp: ENST00000541483.1:c.1623T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968T>C
  hgvsp: ENST00000552103.1:c.1968T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296T>C
  hgvsp: ENST00000545852.1:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968T>C
  hgvsp: ENST00000527509.2:c.1968T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-4041A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12131A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296T>C
  hgvsp: ENST00000424001.1:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296T>C
  hgvsp: ENST00000558540.1:c.1296T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241T>C
  hgvsp: ENST00000423302.2:c.2241T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17756T>C
  variant of: http://identifiers.org/hgnc/14687
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2241T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

11-10603548-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603548
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603548
    reference: chr 11
allele count: 7
allele frequency: 5.818689631095077e-5
allele num: 120302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17771C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12116G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-4026G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-15C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-15C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12239
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

11-10603551-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603551
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603551
    reference: chr 11
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12113G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-4023G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17774C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-18C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-18C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14576
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-5459938-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5459938
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5459939
    reference: chr 7
allele count: 1
allele frequency: 1.369112814895947e-4
allele num: 7304
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-36+4983dupG
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241269
  ensembl transcript: ENST00000342963
  gene symbol: AC093620.5
  hgvsc: ENST00000342963.2:n.152-26dupC
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.187+752dupG
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.187+752dupG
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188365
  ensembl transcript: ENST00000455866
  gene symbol: AC092171.2
  hgvsc: ENST00000455866.1:n.423+42dupC
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1760
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3761
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1263
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

7-5459942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5459942
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5459942
    reference: chr 7
allele count: 83
allele frequency: 1.087241288970396e-2
allele num: 7634
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188365
  ensembl transcript: ENST00000455866
  gene symbol: AC092171.2
  hgvsc: ENST00000455866.1:n.423+43G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241269
  ensembl transcript: ENST00000342963
  gene symbol: AC093620.5
  hgvsc: ENST00000342963.2:n.152-25G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-36+4980C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.187+749C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.187+749C>T
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4746
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3769
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1614
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-5459947-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5459947
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5459947
    reference: chr 7
allele count: 1
allele frequency: 1.238236750866766e-4
allele num: 8076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-36+4975C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188365
  ensembl transcript: ENST00000455866
  gene symbol: AC092171.2
  hgvsc: ENST00000455866.1:n.423+48G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.187+744C>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241269
  ensembl transcript: ENST00000342963
  gene symbol: AC093620.5
  hgvsc: ENST00000342963.2:n.152-20G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.187+744C>T
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2198
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3704
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-5459948-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5459948
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5459948
    reference: chr 7
allele count: 1
allele frequency: 1.223091976516634e-4
allele num: 8176
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.187+743G>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.187+743G>T
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241269
  ensembl transcript: ENST00000342963
  gene symbol: AC093620.5
  hgvsc: ENST00000342963.2:n.152-19C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188365
  ensembl transcript: ENST00000455866
  gene symbol: AC092171.2
  hgvsc: ENST00000455866.1:n.423+49C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-36+4974G>T
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3725
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

7-5459960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5459960
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 5459960
    reference: chr 7
allele count: 1
allele frequency: 1.112099644128114e-4
allele num: 8992
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241269
  ensembl transcript: ENST00000342963
  gene symbol: AC093620.5
  hgvsc: ENST00000342963.2:n.152-7C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382364
  ensembl transcript: ENST00000399434
  gene symbol: TNRC18
  hgvsc: ENST00000399434.2:c.-36+4962G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000395538
  ensembl transcript: ENST00000430969
  gene symbol: TNRC18
  hgvsc: ENST00000430969.1:c.187+731G>A
  variant of: http://identifiers.org/hgnc/11962
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188365
  ensembl transcript: ENST00000455866
  gene symbol: AC092171.2
  hgvsc: ENST00000455866.1:n.423+61C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000182095
  ensembl protein: ENSP00000382452
  ensembl transcript: ENST00000399537
  gene symbol: TNRC18
  hgvsc: ENST00000399537.4:c.187+731G>A
  variant of: http://identifiers.org/hgnc/11962
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3221
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3294
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 2.5e0
  variant carriers: 0
hgvs: n.152-7C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

11-10603551-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603551
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603551
    reference: chr 11
allele count: 1
allele frequency: 8.315455104857889e-6
allele num: 120258
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-4023G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17774C>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-18C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12113G>T
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-10603552-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603552
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603552
    reference: chr 11
allele count: 575
allele frequency: 4.78146620542842e-3
allele num: 120256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17775A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-4022T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12112T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-19A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-19A>G
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13618
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 6.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 9.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
num of homozygotes: 16
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

11-10603563-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603563
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603563
    reference: chr 11
allele count: 2
allele frequency: 1.666388935177471e-5
allele num: 120020
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12101A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17786T>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-4011A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-30T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-30T>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7298
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

11-10603576-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603576
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603576
    reference: chr 11
allele count: 1
allele frequency: 8.363161944267889e-6
allele num: 119572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17799C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-3998G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-43C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12088G>A
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13034
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-10603576-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603576
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603576
    reference: chr 11
allele count: 1
allele frequency: 8.363161944267889e-6
allele num: 119572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17799C>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12088G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-43C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-3998G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-43C>G
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD

11-10603576-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603576
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603576
    reference: chr 11
allele count: 9
allele frequency: 7.526845749841099e-5
allele num: 119572
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12088G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-3998G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17799C>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-43C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-43C>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

11-10603577-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603577
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603577
    reference: chr 11
allele count: 1
allele frequency: 8.370021929457456e-6
allele num: 119474
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-3997T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17800A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-44A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12087T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-44A>G
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12950
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS

11-10603581-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603581
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603581
    reference: chr 11
allele count: 2
allele frequency: 1.677767897589047e-5
allele num: 119206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12083G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-3993G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17804C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-48C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-48C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11278
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

11-10603582-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10603582
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10603582
    reference: chr 11
allele count: 11982
allele frequency: 1.007297060999395e-1
allele num: 118952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-17805C>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1296-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1968-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2160-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1968-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1968-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1296-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*133-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-12082G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1766-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2217-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1296-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2214-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2241-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-3992G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1623-49C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1296-49C>G
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 3.75e1
  variant carriers: 1750
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 11931
  bin: 2.75e1
  variant carriers: 1284
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 412
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 11277
  bin: 3.25e1
  variant carriers: 1630
genotype quality: GenotypeQuality
num of homozygotes: 698
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

11-10613060-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613060
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613060
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 33988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1295+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1622+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2213+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+20054T>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2159+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2604A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1765+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1967+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1295+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1295+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*132+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2216+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1295+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1967+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1967+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2240+35T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2363A>T
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

11-10613061-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613061
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613061
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 34062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1295+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1967+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1967+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+20053A>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1295+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2213+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1295+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1295+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2364T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2240+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2159+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1622+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1967+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*132+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2603T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2216+34A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1765+34A>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

11-10613065-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613065
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613065
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 34614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1765+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*132+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2240+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2599T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1967+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1622+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1967+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1295+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1295+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1295+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2213+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1967+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+20049A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2159+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2368T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2216+30A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1295+30A>G
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28974
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13601
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-10613078-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613078
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613078
    reference: chr 11
allele count: 1
allele frequency: 2.712820791058543e-5
allele num: 36862
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2381A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1295+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2240+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+20036T>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2216+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*132+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1295+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1295+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1622+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2159+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1967+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1967+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2213+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1295+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1967+17T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2586A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1765+17T>G
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9519
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

11-10613083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613083
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613083
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 37764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1295+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1967+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+20031G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1622+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1967+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2216+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2386C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1967+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2213+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*132+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2240+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1295+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1295+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2581C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1295+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1765+12G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2159+12G>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32935
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

11-10613084-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613084
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613084
    reference: chr 11
allele count: 2
allele frequency: 5.24081547088727e-5
allele num: 38162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2387G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1967+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*132+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1295+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2159+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2216+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1967+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2213+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1622+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1295+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2240+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1295+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+20030C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1765+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1295+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2580G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1967+11C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

11-10613138-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613138
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613138
    reference: chr 11
allele count: 1
allele frequency: 2.112646300756327e-5
allele num: 47334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*89G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2170G>A
  hgvsp: ENSP00000414598.1:p.Gly724Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1924G>A
  hgvsp: ENSP00000448278.1:p.Gly642Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2441C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1252G>A
  hgvsp: ENSP00000453013.1:p.Gly418Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1579G>A
  hgvsp: ENSP00000437784.1:p.Gly527Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1252G>A
  hgvsp: ENSP00000401205.1:p.Gly418Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1252G>A
  hgvsp: ENSP00000441971.1:p.Gly418Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.554G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2173G>A
  hgvsp: ENSP00000432436.1:p.Gly725Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2526C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2116G>A
  hgvsp: ENSP00000412229.1:p.Gly706Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19976G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1924G>A
  hgvsp: ENSP00000432067.2:p.Gly642Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1252G>A
  hgvsp: ENSP00000433296.2:p.Gly418Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2197G>A
  hgvsp: ENSP00000412130.2:p.Gly733Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1722G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1924G>A
  hgvsp: ENSP00000446764.1:p.Gly642Ser
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly733Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

11-10613142-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613142
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613142
    reference: chr 11
allele count: 13
allele frequency: 2.759616201069882e-4
allele num: 47108
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1248G>A
  hgvsp: ENST00000558540.1:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1920G>A
  hgvsp: ENST00000552103.1:c.1920G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1920G>A
  hgvsp: ENST00000527509.2:c.1920G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19972G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1248G>A
  hgvsp: ENST00000424001.1:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2166G>A
  hgvsp: ENST00000421747.1:c.2166G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2169G>A
  hgvsp: ENST00000531107.1:c.2169G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1248G>A
  hgvsp: ENST00000545852.1:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2112G>A
  hgvsp: ENST00000436272.1:c.2112G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2193G>A
  hgvsp: ENST00000423302.2:c.2193G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1575G>A
  hgvsp: ENST00000541483.1:c.1575G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1248G>A
  hgvsp: ENST00000534266.2:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1920G>A
  hgvsp: ENST00000547195.1:c.1920G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*85G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2445C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1718G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2522C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.550G>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly731Gly
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-10613143-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613143
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613143
    reference: chr 11
allele count: 1
allele frequency: 2.127659574468085e-5
allele num: 47000
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1919G>C
  hgvsp: ENSP00000448278.1:p.Gly640Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1247G>C
  hgvsp: ENSP00000433296.2:p.Gly416Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*84G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1919G>C
  hgvsp: ENSP00000432067.2:p.Gly640Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2165G>C
  hgvsp: ENSP00000414598.1:p.Gly722Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1247G>C
  hgvsp: ENSP00000441971.1:p.Gly416Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1574G>C
  hgvsp: ENSP00000437784.1:p.Gly525Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2111G>C
  hgvsp: ENSP00000412229.1:p.Gly704Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2168G>C
  hgvsp: ENSP00000432436.1:p.Gly723Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19971G>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1919G>C
  hgvsp: ENSP00000446764.1:p.Gly640Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1247G>C
  hgvsp: ENSP00000453013.1:p.Gly416Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1247G>C
  hgvsp: ENSP00000401205.1:p.Gly416Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2521C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2192G>C
  hgvsp: ENSP00000412130.2:p.Gly731Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1717G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.549G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2446C>G
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly731Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-10613143-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613143
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613143
    reference: chr 11
allele count: 2
allele frequency: 4.25531914893617e-5
allele num: 47000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1919G>A
  hgvsp: ENSP00000432067.2:p.Gly640Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1247G>A
  hgvsp: ENSP00000433296.2:p.Gly416Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1717G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2168G>A
  hgvsp: ENSP00000432436.1:p.Gly723Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1247G>A
  hgvsp: ENSP00000441971.1:p.Gly416Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2111G>A
  hgvsp: ENSP00000412229.1:p.Gly704Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2521C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19971G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1919G>A
  hgvsp: ENSP00000446764.1:p.Gly640Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2192G>A
  hgvsp: ENSP00000412130.2:p.Gly731Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2165G>A
  hgvsp: ENSP00000414598.1:p.Gly722Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1247G>A
  hgvsp: ENSP00000401205.1:p.Gly416Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*84G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1574G>A
  hgvsp: ENSP00000437784.1:p.Gly525Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.549G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2446C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1919G>A
  hgvsp: ENSP00000448278.1:p.Gly640Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1247G>A
  hgvsp: ENSP00000453013.1:p.Gly416Glu
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly731Glu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

11-10613146-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613146
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613146
    reference: chr 11
allele count: 2
allele frequency: 4.261484701269923e-5
allele num: 46932
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2162A>G
  hgvsp: ENSP00000414598.1:p.Asn721Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*81A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2165A>G
  hgvsp: ENSP00000432436.1:p.Asn722Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2518T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2108A>G
  hgvsp: ENSP00000412229.1:p.Asn703Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19968A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1244A>G
  hgvsp: ENSP00000453013.1:p.Asn415Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1244A>G
  hgvsp: ENSP00000441971.1:p.Asn415Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1916A>G
  hgvsp: ENSP00000432067.2:p.Asn639Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1916A>G
  hgvsp: ENSP00000448278.1:p.Asn639Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1244A>G
  hgvsp: ENSP00000433296.2:p.Asn415Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.546A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2189A>G
  hgvsp: ENSP00000412130.2:p.Asn730Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1571A>G
  hgvsp: ENSP00000437784.1:p.Asn524Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2449T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1916A>G
  hgvsp: ENSP00000446764.1:p.Asn639Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1714A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1244A>G
  hgvsp: ENSP00000401205.1:p.Asn415Ser
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn730Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-10613158-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613158
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613158
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 45060
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2153C>T
  hgvsp: ENSP00000432436.1:p.Ser718Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2177C>T
  hgvsp: ENSP00000412130.2:p.Ser726Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1232C>T
  hgvsp: ENSP00000441971.1:p.Ser411Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19956C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2096C>T
  hgvsp: ENSP00000412229.1:p.Ser699Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.534C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2506G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1559C>T
  hgvsp: ENSP00000437784.1:p.Ser520Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2461G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2150C>T
  hgvsp: ENSP00000414598.1:p.Ser717Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1232C>T
  hgvsp: ENSP00000433296.2:p.Ser411Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1232C>T
  hgvsp: ENSP00000453013.1:p.Ser411Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1232C>T
  hgvsp: ENSP00000401205.1:p.Ser411Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1904C>T
  hgvsp: ENSP00000446764.1:p.Ser635Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1904C>T
  hgvsp: ENSP00000432067.2:p.Ser635Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*69C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1702C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1904C>T
  hgvsp: ENSP00000448278.1:p.Ser635Leu
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser726Leu
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-10613162-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613162
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613162
    reference: chr 11
allele count: 9
allele frequency: 2.017484868863483e-4
allele num: 44610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1701-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.533-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2152-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1558-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*68-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2095-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2149-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1231-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1231-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1903-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1903-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1903-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2502G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1231-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2465G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19952C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2176-3C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1231-3C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2176-3C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

11-10613173-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613173
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613173
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 42210
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2176-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1231-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*68-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19941T>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1903-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2149-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1231-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1231-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2491A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1903-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2152-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2095-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.533-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1701-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1558-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.485+2476A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1231-14T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1903-14T>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/11-10613184-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613184
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613184
    reference: chr 11
allele count: 2
allele frequency: 4.970920117313715e-5
allele num: 40234
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2095-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.533-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2176-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2149-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1903-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2152-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*68-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1558-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1231-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1231-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19930T>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1231-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1903-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1701-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1903-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-2480A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1231-25T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2480A>C
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14720
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-10613195-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613195
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613195
    reference: chr 11
allele count: 2
allele frequency: 5.586280096084018e-5
allele num: 35802
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2149-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.533-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1231-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1903-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1231-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1231-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2176-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1231-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2469C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1903-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2095-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1558-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2152-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19919G>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-2469C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*68-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1903-36G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1701-36G>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6323
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17060
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP

11-10613195-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613195
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613195
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 35802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2149-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1701-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.533-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2469C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2095-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*68-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1231-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1903-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1903-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2176-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19919G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1231-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-2469C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1558-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1231-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1231-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1903-36G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2152-36G>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17060
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

11-10613196-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10613196
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10613196
    reference: chr 11
allele count: 9
allele frequency: 2.557980900409277e-4
allele num: 35184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1903-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2149-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-2468G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1231-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1903-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1231-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2095-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1701-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-2468G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1903-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+19918C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1231-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.533-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2176-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1231-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1558-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*68-37C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2152-37C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1404
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/11-10614989-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10614989
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10614989
    reference: chr 11
allele count: 1
allele frequency: 8.531986417077625e-6
allele num: 117206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-675A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.246A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18125T>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-675A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+50T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+50T>G
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

11-10614989-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10614989
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10614989
    reference: chr 11
allele count: 1557
allele frequency: 1.328430285138986e-2
allele num: 117206
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-675A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.246A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18125T>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-675A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+50T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+50T>A
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 7.5e0
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3917
  bin: 3.25e1
  variant carriers: 127
genotype quality: GenotypeQuality
num of homozygotes: 17
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

11-10614996-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10614996
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10614996
    reference: chr 11
allele count: 1
allele frequency: 8.507307777380771e-6
allele num: 117546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18118T>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.253A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-668A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-668A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+43T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+43T>A
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-10614998-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10614998
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10614998
    reference: chr 11
allele count: 1
allele frequency: 8.498342823149486e-6
allele num: 117670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-666T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-666T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.255T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18116A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+41A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+41A>G
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

11-10614998-TCTA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10614998
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10614995
    reference: chr 11
allele count: 2
allele frequency: 1.699668564629897e-5
allele num: 117670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+38_1902+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+38_1230+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+38_2151+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+38_*67+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+38_1230+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+38_2148+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+38_1230+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+38_2175+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+38_1902+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-662_486-660delCTA
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-662_272-660delCTA
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18113_123+18115delTAG
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+38_532+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.259_261delCTA
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+38_1902+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+38_2094+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+38_1230+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+38_*1700+40delTAG
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+38_1557+40delTAG
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: TCTA
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-10615002-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615002
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615002
    reference: chr 11
allele count: 1
allele frequency: 8.500076500688507e-6
allele num: 117646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.259C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-662C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-662C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18112G>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+37G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+37G>C
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-10615005-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615005
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615005
    reference: chr 11
allele count: 10
allele frequency: 8.47658766486963e-5
allele num: 117972
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18109A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.262T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+34A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-659T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-659T>C
  variant of: http://identifiers.org/hgnc/43434
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13351
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

11-10615011-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615011
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615011
    reference: chr 11
allele count: 1
allele frequency: 8.433125316242199e-6
allele num: 118580
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-653G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18103C>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.268G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-653G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+28C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+28C>G
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

11-10615015-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615015
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615015
    reference: chr 11
allele count: 4
allele frequency: 3.359537727608681e-5
allele num: 119064
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.272G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18099C>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-649G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-649G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+24C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+24C>G
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14908
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-10615020-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615020
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615020
    reference: chr 11
allele count: 1
allele frequency: 8.371983992766606e-6
allele num: 119446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18094G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.277C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-644C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-644C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+19G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+19G>A
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-10615027-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615027
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615027
    reference: chr 11
allele count: 11
allele frequency: 9.164375572773474e-5
allele num: 120030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.284C>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18087G>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-637C>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-637C>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+12G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+12G>T
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-10615028-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615028
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615028
    reference: chr 11
allele count: 3
allele frequency: 2.496837339370131e-5
allele num: 120152
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.285G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18086C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-636G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-636G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+11C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+11C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4660
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

11-10615031-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615031
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615031
    reference: chr 11
allele count: 3
allele frequency: 2.492398185534121e-5
allele num: 120366
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-633A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-633A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18083T>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+8T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.288A>T
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2175+8T>A
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-10615036-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615036
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615036
    reference: chr 11
allele count: 1
allele frequency: 8.29655195300833e-6
allele num: 120532
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1230+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.532+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1230+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1557+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18078A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2175+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1230+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2148+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2151+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2094+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*67+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1902+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1902+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.293T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-628T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1902+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1700+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1230+3A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-628T>C
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.2175+3A>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-10615055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615055
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615055
    reference: chr 11
allele count: 1
allele frequency: 8.266785708380868e-6
allele num: 120966
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1214C>T
  hgvsp: ENSP00000453013.1:p.Pro405Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1684C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1214C>T
  hgvsp: ENSP00000401205.1:p.Pro405Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1886C>T
  hgvsp: ENSP00000432067.2:p.Pro629Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-609G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1214C>T
  hgvsp: ENSP00000433296.2:p.Pro405Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.516C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1541C>T
  hgvsp: ENSP00000437784.1:p.Pro514Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1886C>T
  hgvsp: ENSP00000446764.1:p.Pro629Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2135C>T
  hgvsp: ENSP00000432436.1:p.Pro712Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.303+9G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2132C>T
  hgvsp: ENSP00000414598.1:p.Pro711Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*51C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2078C>T
  hgvsp: ENSP00000412229.1:p.Pro693Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18059C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1886C>T
  hgvsp: ENSP00000448278.1:p.Pro629Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2159C>T
  hgvsp: ENSP00000412130.2:p.Pro720Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-609G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1214C>T
  hgvsp: ENSP00000441971.1:p.Pro405Leu
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro720Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

11-10615103-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615103
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615103
    reference: chr 11
allele count: 5
allele frequency: 4.123915410247105e-5
allele num: 121244
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2084T>C
  hgvsp: ENSP00000414598.1:p.Phe695Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1166T>C
  hgvsp: ENSP00000441971.1:p.Phe389Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2030T>C
  hgvsp: ENSP00000412229.1:p.Phe677Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1838T>C
  hgvsp: ENSP00000448278.1:p.Phe613Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1838T>C
  hgvsp: ENSP00000432067.2:p.Phe613Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18011T>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2111T>C
  hgvsp: ENSP00000412130.2:p.Phe704Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1166T>C
  hgvsp: ENSP00000453013.1:p.Phe389Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1493T>C
  hgvsp: ENSP00000437784.1:p.Phe498Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-561A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1166T>C
  hgvsp: ENSP00000401205.1:p.Phe389Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2087T>C
  hgvsp: ENSP00000432436.1:p.Phe696Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1636T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1838T>C
  hgvsp: ENSP00000446764.1:p.Phe613Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1166T>C
  hgvsp: ENSP00000433296.2:p.Phe389Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.468T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.*3T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-561A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.303+57A>G
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe704Ser
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-10615109-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10615109
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10615109
    reference: chr 11
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-555G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.1832C>T
  hgvsp: ENSP00000448278.1:p.Pro611Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1160C>T
  hgvsp: ENSP00000401205.1:p.Pro387Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1160C>T
  hgvsp: ENSP00000453013.1:p.Pro387Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.1832C>T
  hgvsp: ENSP00000446764.1:p.Pro611Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1160C>T
  hgvsp: ENSP00000433296.2:p.Pro387Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1160C>T
  hgvsp: ENSP00000441971.1:p.Pro387Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1487C>T
  hgvsp: ENSP00000437784.1:p.Pro496Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.1832C>T
  hgvsp: ENSP00000432067.2:p.Pro611Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000072952
  ensembl transcript: ENST00000529471
  gene symbol: MRVI1
  hgvsc: ENST00000529471.1:n.462C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2078C>T
  hgvsp: ENSP00000414598.1:p.Pro693Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2081C>T
  hgvsp: ENSP00000432436.1:p.Pro694Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2024C>T
  hgvsp: ENSP00000412229.1:p.Pro675Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000435658
  ensembl transcript: ENST00000526414
  gene symbol: MRVI1
  hgvsc: ENST00000526414.1:c.1284C>T
  hgvsp: ENST00000526414.1:c.1284C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2105C>T
  hgvsp: ENSP00000412130.2:p.Pro702Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000525578
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000525578.1:n.303+63G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.486-555G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1630C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.123+18005C>T
  variant of: http://identifiers.org/hgnc/14687
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
hgvs: p.Pro702Leu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 10502
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 94
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.25e-2

DP
type: SiteQuality
SIO_000300: 5.32986e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.983e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.458e-1

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.471e0

QD
type: SiteQuality
SIO_000300: 8.26e0

DP
type: SiteQuality
SIO_000300: 5.08806e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.09e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.484e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

GenotypeQuality
all individuals: 3076
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 219
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3047
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.263264274886306e-4
allele num: 7916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2032
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.126633618747183e-4
allele num: 8876
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.09e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.471e0

DP
type: SiteQuality
SIO_000300: 5.08806e5

FS
type: SiteQuality
SIO_000300: 6.484e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

QD
type: SiteQuality
SIO_000300: 8.26e0

GenotypeQuality
all individuals: 275
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 378
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1986
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.267105930055753e-4
allele num: 7892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

QD
type: SiteQuality
SIO_000300: 1.072e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

FS
type: SiteQuality
SIO_000300: 2.578e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.456e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 4.78617e5

GenotypeQuality
all individuals: 22
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.555555555555556e-3
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 9.501187648456057e-4
allele num: 8420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.267105930055753e-4
allele num: 7892
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

FS
type: SiteQuality
SIO_000300: 2.578e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.456e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 4.78617e5

QD
type: SiteQuality
SIO_000300: 1.072e1

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

GenotypeQuality
all individuals: 657
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2489
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 9.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
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East Asian
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South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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FS
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QD
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MQ
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VQSLOD
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ClippingRankSum
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DP
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BaseQRankSum
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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

East Asian
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allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.581311306143521e-4
allele num: 7748
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 1898
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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SIO_000300: -7.9e-2

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

GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 160
num of homozygotes: 0

African
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South Asian
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allele frequency: 1.27942681678608e-4
allele num: 7816
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 6726
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Latino
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allele frequency: 0.0e0
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East Asian
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QD
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SIO_000300: 9.119999999999999e0

ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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MQ
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BaseQRankSum
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FS
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SIO_000300: 3.444e0

ReadPosRankSum
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SIO_000300: 1.03e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5862
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African
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East Asian
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allele frequency: 0.0e0
allele num: 316
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South Asian
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allele frequency: 1.288659793814433e-4
allele num: 7760
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
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ClippingRankSum
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.913e1

InbreedingCoeff
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SIO_000300: -9.73e-2

DP
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SIO_000300: 3.75394e5

BaseQRankSum
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SIO_000300: 7.27e-1

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 224

GenotypeQuality
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South Asian
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allele count: 192
allele frequency: 4.21792618629174e-2
allele num: 4552
num of homozygotes: 6

European (Non-Finnish)
type: Population
allele count: 38
allele frequency: 2.398989898989899e-2
allele num: 1584
num of homozygotes: 0

East Asian
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allele frequency: 5.737704918032787e-2
allele num: 122
num of homozygotes: 0

African
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allele count: 13
allele frequency: 9.154929577464789e-2
allele num: 142
num of homozygotes: 1

Other
type: Population
allele count: 2
allele frequency: 3.225806451612903e-2
allele num: 62
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 3.703703703703703e-2
allele num: 54
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.852e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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SIO_000300: 1.408e1

DP
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SIO_000300: 7.2703e4

GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: NaN
allele num: 0
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South Asian
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African
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

Other
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
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SIO_000300: -6.54e-2

MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 7.4423e4

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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VQSLOD
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SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.998770504093322e-5
allele num: 66694
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11572
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 898
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DP
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SIO_000300: 1.965454e6

BaseQRankSum
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MQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-3

QD
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SIO_000300: 1.217e1

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 1
allele frequency: 1.514233797698365e-4
allele num: 6604
num of homozygotes: 0

Other
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East Asian
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Latino
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allele frequency: 8.647526807333103e-5
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African
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allele frequency: 1.020616452337212e-4
allele num: 9798
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 71
allele frequency: 1.065426170468187e-3
allele num: 66640
num of homozygotes: 0

VQSLOD
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FS
type: SiteQuality
SIO_000300: 6.43e-1

BaseQRankSum
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DP
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

Latino
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East Asian
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African
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Other
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South Asian
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European (Finnish)
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ReadPosRankSum
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SIO_000300: -1.1e-1

VQSLOD
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MQ
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BaseQRankSum
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QD
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FS
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele frequency: 1.353505579450778e-4
allele num: 66494
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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Other
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allele num: 890
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African
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allele frequency: 5.58505207269757e-2
allele num: 9794
num of homozygotes: 16

South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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MQ
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VQSLOD
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DP
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 1.169043722235212e-4
allele num: 8554
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Other
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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: 1.506704836522525e-5
allele num: 66370
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

East Asian
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allele frequency: 1.17813383600377e-4
allele num: 8488
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Latino
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allele count: 0
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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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num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 3.471619510501649e-4
allele num: 11522
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African
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European (Non-Finnish)
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allele count: 5
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allele num: 66160
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Other
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QD
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MQRankSum
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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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MQ
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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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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African
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East Asian
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allele frequency: 1.179801793298726e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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MQRankSum
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VQSLOD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Non-Finnish)
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Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 677

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 32

European (Non-Finnish)
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allele count: 7159
allele frequency: 1.086936718085752e-1
allele num: 65864
num of homozygotes: 417

African
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allele frequency: 8.74820733456259e-2
allele num: 9762
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Latino
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allele frequency: 1.202443280977312e-1
allele num: 11460
num of homozygotes: 95

East Asian
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allele count: 76
allele frequency: 9.039010466222646e-3
allele num: 8408
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European (Finnish)
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allele count: 938
allele frequency: 1.429442243218531e-1
allele num: 6562
num of homozygotes: 55

South Asian
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allele count: 1501
allele frequency: 9.370707953552254e-2
allele num: 16018
num of homozygotes: 90

Other
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allele count: 76
allele frequency: 8.656036446469248e-2
allele num: 878
num of homozygotes: 1

FS
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SIO_000300: 0.0e0

VQSLOD
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MQ
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BaseQRankSum
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QD
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InbreedingCoeff
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SIO_000300: 1.35e-2

ReadPosRankSum
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SIO_000300: 2.43e-1

ClippingRankSum
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SIO_000300: -2.41e-1

DP
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SIO_000300: 2.001747e6

MQRankSum
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SIO_000300: 3.9e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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East Asian
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African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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European (Finnish)
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ClippingRankSum
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SIO_000300: 1.22e0

DP
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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East Asian
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South Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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MQ
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MQRankSum
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FS
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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MQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQRankSum
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FS
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VQSLOD
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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South Asian
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MQ
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ReadPosRankSum
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MQRankSum
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DP
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Finnish)
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Other
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European (Non-Finnish)
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MQ
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ClippingRankSum
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DP
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FS
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QD
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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East Asian
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South Asian
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African
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European (Non-Finnish)
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Latino
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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East Asian
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African
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European (Finnish)
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Other
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MQ
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QD
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DP
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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East Asian
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South Asian
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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QD
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MQRankSum
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FS
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 2
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allele num: 25246
num of homozygotes: 0

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 2

GenotypeQuality
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variant carriers: 1541

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 2003
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variant carriers: 2

GenotypeQuality
all individuals: 2932
bin: 3.25e1
variant carriers: 1

African
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allele count: 13
allele frequency: 1.353039134054954e-3
allele num: 9608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1230
allele frequency: 1.894406111384919e-2
allele num: 64928
num of homozygotes: 9

Latino
type: Population
allele count: 41
allele frequency: 3.673835125448029e-3
allele num: 11160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 203
allele frequency: 3.118279569892473e-2
allele num: 6510
num of homozygotes: 6

Other
type: Population
allele count: 18
allele frequency: 2.064220183486239e-2
allele num: 872
num of homozygotes: 0

South Asian
type: Population
allele count: 52
allele frequency: 3.309572301425662e-3
allele num: 15712
num of homozygotes: 2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.33e0

QD
type: SiteQuality
SIO_000300: 1.843e1

MQRankSum
type: SiteQuality
SIO_000300: 1.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

DP
type: SiteQuality
SIO_000300: 1.51414e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 656
bin: 5.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1918
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GenotypeQuality
all individuals: 1912
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2345
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GenotypeQuality
all individuals: 1757
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15736
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11192
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.534354190321294e-5
allele num: 65174
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.866e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.116e0

DP
type: SiteQuality
SIO_000300: 1.536606e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.281e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

QD
type: SiteQuality
SIO_000300: 7.35e0

GenotypeDepth
all individuals: 182
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6928
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variant carriers: 0

GenotypeDepth
all individuals: 655
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variant carriers: 0

GenotypeDepth
all individuals: 21500
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variant carriers: 0

GenotypeDepth
all individuals: 98
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variant carriers: 0

GenotypeDepth
all individuals: 1520
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variant carriers: 0

GenotypeDepth
all individuals: 203
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variant carriers: 0

GenotypeDepth
all individuals: 419
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variant carriers: 0

GenotypeDepth
all individuals: 262
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variant carriers: 0

GenotypeDepth
all individuals: 12286
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GenotypeDepth
all individuals: 158
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variant carriers: 0

GenotypeDepth
all individuals: 4001
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GenotypeDepth
all individuals: 121
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GenotypeDepth
all individuals: 569
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GenotypeDepth
all individuals: 830
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 2096
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3319
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GenotypeQuality
all individuals: 195
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1916
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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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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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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
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variant carriers: 0

GenotypeQuality
all individuals: 5230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1583
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533083951677194e-5
allele num: 65228
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9638
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15760
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

FS
type: SiteQuality
SIO_000300: 3.802e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

DP
type: SiteQuality
SIO_000300: 1.547445e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeDepth
all individuals: 655
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 569
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variant carriers: 0

GenotypeDepth
all individuals: 830
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 158
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variant carriers: 0

GenotypeDepth
all individuals: 1520
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GenotypeDepth
all individuals: 1614
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variant carriers: 0

GenotypeDepth
all individuals: 7331
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variant carriers: 0

GenotypeDepth
all individuals: 586
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variant carriers: 0

GenotypeDepth
all individuals: 4001
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variant carriers: 0

GenotypeDepth
all individuals: 6928
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 1768
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variant carriers: 0

GenotypeQuality
all individuals: 3744
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 2.75e1
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GenotypeQuality
all individuals: 5309
bin: 9.75e1
variant carriers: 2

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
all individuals: 712
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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: 3319
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1916
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1917
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variant carriers: 0

GenotypeQuality
all individuals: 26375
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1583
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11208
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8434
num of homozygotes: 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: 9638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.066167903354387e-5
allele num: 65228
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

DP
type: SiteQuality
SIO_000300: 1.547445e6

FS
type: SiteQuality
SIO_000300: 3.802e0

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.93e-1

BaseQRankSum
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SIO_000300: 1.1e0

VQSLOD
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SIO_000300: 2.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

QD
type: SiteQuality
SIO_000300: 1.209e1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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bin: 3.75e1
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 711
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5306
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1883
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1734
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 859
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variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65194
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.348400203148806e-5
allele num: 15752
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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.543e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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SIO_000300: 1.55e-1

ClippingRankSum
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SIO_000300: 8.110000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.576578e6

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 532
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variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 5
allele frequency: 3.157761778451434e-4
allele num: 15834
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.120887528691661e-5
allele num: 65350
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 8.890469416785207e-5
allele num: 11248
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 9.0e-4

FS
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SIO_000300: 0.0e0

VQSLOD
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BaseQRankSum
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SIO_000300: 2.19e0

MQRankSum
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SIO_000300: 1.8e-1

DP
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -7.02e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele count: 0
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

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

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

African
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allele count: 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: 1.522718966987453e-5
allele num: 65672
num of homozygotes: 0

East Asian
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num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 7.41e-1

BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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MQRankSum
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FS
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SIO_000300: 6.327e0

QD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.068697657482704e-5
allele num: 65912
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8574
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.929999999999999e-1

DP
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SIO_000300: 1.658931e6

BaseQRankSum
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SIO_000300: 3.81e-1

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.422e1

FS
type: SiteQuality
SIO_000300: 6.232e0

MQRankSum
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ReadPosRankSum
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SIO_000300: -2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele frequency: 6.203473945409429e-5
allele num: 16120
num of homozygotes: 0

European (Non-Finnish)
type: Population
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allele frequency: 0.0e0
allele num: 66094
num of homozygotes: 0

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

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

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

Latino
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MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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QD
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VQSLOD
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 1

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

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: 8
allele frequency: 1.205836247437598e-4
allele num: 66344
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.750437521876094e-5
allele num: 11428
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.022653721682848e-4
allele num: 9888
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

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

African
type: Population
allele count: 1
allele frequency: 1.009081735620585e-4
allele num: 9910
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506205566935775e-5
allele num: 66392
num of homozygotes: 0

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

South Asian
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European (Non-Finnish)
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Other
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Latino
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African
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European (Finnish)
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ClippingRankSum
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MQ
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MQRankSum
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FS
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VQSLOD
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DP
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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African
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Latino
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European (Finnish)
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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DP
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ClippingRankSum
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Non-Finnish)
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East Asian
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Latino
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European (Finnish)
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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FS
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QD
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BaseQRankSum
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ReadPosRankSum
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