http://identifiers.org/exac.variant/19-2269548-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269548
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269548
    reference: chr 19
allele count: 1
allele frequency: 1.146788990825688e-4
allele num: 8720
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-50C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-50C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.151G>T
  hgvsp: ENSP00000465604.2:p.Ala51Ser
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-50C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.20C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-50C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-50C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.35C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.1C>A
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28797
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala51Ser
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD

19-2269548-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269548
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269548
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 8720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.20C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-50C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.35C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-50C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.151G>A
  hgvsp: ENSP00000465604.2:p.Ala51Thr
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-50C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.1C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-50C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-50C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28797
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22949
  bin: 7.5e0
  variant carriers: 1
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: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2449
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27410
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala51Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

19-2269551-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269551
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269551
    reference: chr 19
allele count: 1
allele frequency: 9.848335631278314e-5
allele num: 10154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-47G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.23G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.4G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-47G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-47G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-47G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.148C>G
  hgvsp: ENSP00000465604.2:p.Arg50Gly
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.38G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-47G>C
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25232
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1192
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg50Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

19-2269551-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269551
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269551
    reference: chr 19
allele count: 1
allele frequency: 9.848335631278314e-5
allele num: 10154
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-47G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-47G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.148C>A
  hgvsp: ENSP00000465604.2:p.Arg50Ser
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.4G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-47G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-47G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-47G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.23G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.38G>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25755
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 1.25e1
  variant carriers: 0
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: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26206
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1525
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg50Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum

19-2269552-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269552
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269552
    reference: chr 19
allele count: 18
allele frequency: 1.675665611617948e-3
allele num: 10742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-46G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.147C>A
  hgvsp: ENST00000593238.2:c.147C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.24G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-46G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.5G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-46G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.39G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-46G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-46G>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26482
  bin: 7.5e0
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25516
  bin: 2.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24288
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 24540
  bin: 7.5e0
  variant carriers: 5
hgvs: p.Leu49Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

19-2269553-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269553
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269553
    reference: chr 19
allele count: 2
allele frequency: 1.808318264014467e-4
allele num: 11060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-45A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-45A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.40A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.146T>C
  hgvsp: ENSP00000465604.2:p.Leu49Pro
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-45A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-45A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.25A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.6A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-45A>G
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24592
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  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 depth: GenotypeDepth
  all individuals: 140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu49Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-2269554-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269554
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269554
    reference: chr 19
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-44G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-44G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-44G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.41G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-44G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-44G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.145C>G
  hgvsp: ENSP00000465604.2:p.Leu49Val
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.7G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.26G>C
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24003
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 827
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26050
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu49Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/19-2269555-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269555
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269555
    reference: chr 19
allele count: 2
allele frequency: 1.69606512890095e-4
allele num: 11792
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-43A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.144T>G
  hgvsp: ENST00000593238.2:c.144T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-43A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.8A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.27A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-43A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-43A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-43A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.42A>C
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28763
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22430
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26958
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser48Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum

19-2269555-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269555
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269555
    reference: chr 19
allele count: 1
allele frequency: 8.480325644504748e-5
allele num: 11792
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-43A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-43A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-43A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.144T>C
  hgvsp: ENST00000593238.2:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.27A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.8A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-43A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.42A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-43A>G
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  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: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22430
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2506
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser48Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-2269556-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269556
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269556
    reference: chr 19
allele count: 1
allele frequency: 8.176614881439084e-5
allele num: 12230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-42G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-42G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-42G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.43G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-42G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-42G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.143C>T
  hgvsp: ENSP00000465604.2:p.Ser48Phe
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.28G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.9G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  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: 22554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.75e1
  variant carriers: 0
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: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27579
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21759
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1022
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser48Phe
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-2269557-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269557
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269557
    reference: chr 19
allele count: 1
allele frequency: 8.01538954793203e-5
allele num: 12476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-41A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.10A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-41A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-41A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.142T>C
  hgvsp: ENSP00000465604.2:p.Ser48Pro
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-41A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-41A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.44A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.29A>G
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22041
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29853
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  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 quality: GenotypeQuality
  all individuals: 2819
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28102
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21289
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser48Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

19-2269558-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269558
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269558
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 12790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-40C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-40C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.30C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.45C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-40C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-40C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.141G>C
  hgvsp: ENST00000593238.2:c.141G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-40C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.11C>G
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30450
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20585
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28708
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala47Ala
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

19-2269558-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269558
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269558
    reference: chr 19
allele count: 2
allele frequency: 1.563721657544957e-4
allele num: 12790
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-40C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.11C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.45C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-40C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-40C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.141G>A
  hgvsp: ENST00000593238.2:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.30C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-40C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-40C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30450
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28708
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala47Ala
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

19-2269560-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269560
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269560
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 14034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.139G>A
  hgvsp: ENSP00000465604.2:p.Ala47Thr
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.32C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.13C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.47C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-38C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31605
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19146
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala47Thr
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: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS

19-2269561-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269561
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269561
    reference: chr 19
allele count: 1
allele frequency: 6.754018641091449e-5
allele num: 14806
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.138T>C
  hgvsp: ENST00000593238.2:c.138T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-37A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.33A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.14A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.48A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-37A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-37A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-37A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-37A>G
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18892
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.25e1
  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: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32322
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30827
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala46Ala
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

19-2269561-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269561
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269561
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 14806
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.14A>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-37A>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.33A>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-37A>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-37A>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.138T>A
  hgvsp: ENST00000593238.2:c.138T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-37A>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.48A>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-37A>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18892
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  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: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30827
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Ala46Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS

19-2269562-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269562
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269562
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 15308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-36G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-36G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-36G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-36G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.137C>T
  hgvsp: ENSP00000465604.2:p.Ala46Val
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-36G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.49G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.34G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.15G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32871
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  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: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3896
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala46Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

19-2269563-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269563
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269563
    reference: chr 19
allele count: 83
allele frequency: 5.221439355812783e-3
allele num: 15896
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-35C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-35C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.50C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.136G>C
  hgvsp: ENSP00000465604.2:p.Ala46Pro
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-35C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.16C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-35C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.35C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-35C>G
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33405
  bin: 7.5e0
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 1.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17263
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16773
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 1.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala46Pro
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

19-2269563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269563
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269563
    reference: chr 19
allele count: 2
allele frequency: 1.258178158027177e-4
allele num: 15896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.136G>A
  hgvsp: ENSP00000465604.2:p.Ala46Thr
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-35C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-35C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-35C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.50C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.35C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.16C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-35C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-35C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33405
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17263
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31711
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala46Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

19-2269564-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269564
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269564
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 16980
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.17G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-34G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-34G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.135C>T
  hgvsp: ENST00000593238.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-34G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-34G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.51G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-34G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.36G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34019
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.75e1
  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: 2873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
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: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15889
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1080
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser45Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

19-2269564-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269564
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269564
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 16980
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-34G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.51G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.36G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.17G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-34G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-34G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-34G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.135C>G
  hgvsp: ENST00000593238.2:c.135C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-34G>C
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34019
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16319
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4504
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32607
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser45Ser
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

19-2269567-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269567
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269567
    reference: chr 19
allele count: 1
allele frequency: 5.330490405117271e-5
allele num: 18760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.54G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.20G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-31G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-31G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.132C>G
  hgvsp: ENST00000593238.2:c.132C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-31G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-31G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-31G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.39G>C
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 1.75e1
  variant carriers: 1
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: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr44Thr
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

19-2269572-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269572
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269572
    reference: chr 19
allele count: 4
allele frequency: 1.783803068141277e-4
allele num: 22424
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.59T>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-26T>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-26T>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.44T>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.25T>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-26T>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-26T>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.127A>C
  hgvsp: ENSP00000465604.2:p.Lys43Gln
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-26T>G
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3583
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35976
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys43Gln
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

19-2269581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269581
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269581
    reference: chr 19
allele count: 1
allele frequency: 3.662735330745e-5
allele num: 27302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-17C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-17C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.53C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.68C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.34C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.118G>A
  hgvsp: ENSP00000465604.2:p.Glu40Lys
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-17C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-17C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4159
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8881
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33859
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu40Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-2269586-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269586
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269586
    reference: chr 19
allele count: 1
allele frequency: 3.106554830692762e-5
allele num: 32190
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-12C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.39C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.113G>C
  hgvsp: ENSP00000465604.2:p.Gly38Ala
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-12C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-12C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.73C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-12C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.58C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-12C>G
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly38Ala
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

19-2269586-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269586
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269586
    reference: chr 19
allele count: 1
allele frequency: 3.106554830692762e-5
allele num: 32190
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.39C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.-12C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.113G>A
  hgvsp: ENSP00000465604.2:p.Gly38Glu
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.-12C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.-12C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.-12C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.-12C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.73C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.58C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly38Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/19-2269605-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269605
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269605
    reference: chr 19
allele count: 1
allele frequency: 2.0755500207555e-5
allele num: 48180
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.8A>C
  hgvsp: ENSP00000314813.4:p.Lys3Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.8A>C
  hgvsp: ENSP00000463955.3:p.Lys3Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.8A>C
  hgvsp: ENSP00000464146.3:p.Lys3Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.8A>C
  hgvsp: ENSP00000467452.1:p.Lys3Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.58A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.8A>C
  hgvsp: ENSP00000473381.1:p.Lys3Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.92A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.77A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.94T>G
  hgvsp: ENSP00000465604.2:p.Phe32Val
  variant of: http://identifiers.org/hgnc/24963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31887
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4871
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Lys3Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

19-2269611-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269611
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269611
    reference: chr 19
allele count: 1
allele frequency: 1.979022362952701e-5
allele num: 50530
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.98C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.14C>T
  hgvsp: ENSP00000473381.1:p.Ser5Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.83C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.14C>T
  hgvsp: ENSP00000464146.3:p.Ser5Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.88G>A
  hgvsp: ENSP00000465604.2:p.Glu30Lys
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.14C>T
  hgvsp: ENSP00000467452.1:p.Ser5Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.14C>T
  hgvsp: ENSP00000314813.4:p.Ser5Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.64C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.14C>T
  hgvsp: ENSP00000463955.3:p.Ser5Phe
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser5Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum

19-2269612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269612
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269612
    reference: chr 19
allele count: 1
allele frequency: 1.962169374460403e-5
allele num: 50964
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.15C>T
  hgvsp: ENST00000582888.4:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.84C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.65C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.15C>T
  hgvsp: ENST00000590943.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.15C>T
  hgvsp: ENST00000322297.4:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.15C>T
  hgvsp: ENST00000583542.4:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.99C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.87G>A
  hgvsp: ENST00000593238.2:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.15C>T
  hgvsp: ENST00000602676.2:c.15C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser5Ser
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: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

19-2269639-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269639
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269639
    reference: chr 19
allele count: 1
allele frequency: 1.76385508166649e-5
allele num: 56694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.42C>T
  hgvsp: ENST00000582888.4:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.42C>T
  hgvsp: ENST00000322297.4:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.60G>A
  hgvsp: ENST00000593238.2:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.42C>T
  hgvsp: ENST00000583542.4:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.42C>T
  hgvsp: ENST00000590943.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.42C>T
  hgvsp: ENST00000602676.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.126C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.92C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.111C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  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: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys14Cys
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-2269642-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269642
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269642
    reference: chr 19
allele count: 1
allele frequency: 1.758458183864388e-5
allele num: 56868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.114C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.129C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.95C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.45C>T
  hgvsp: ENST00000583542.4:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.45C>T
  hgvsp: ENST00000590943.2:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.57G>A
  hgvsp: ENST00000593238.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.45C>T
  hgvsp: ENST00000602676.2:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.45C>T
  hgvsp: ENST00000582888.4:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.45C>T
  hgvsp: ENST00000322297.4:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7730
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29979
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 764
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe15Phe
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

19-2269649-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269649
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269649
    reference: chr 19
allele count: 1
allele frequency: 1.740341106856944e-5
allele num: 57460
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.52G>C
  hgvsp: ENSP00000463955.3:p.Glu18Gln
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.52G>C
  hgvsp: ENSP00000473381.1:p.Glu18Gln
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.52G>C
  hgvsp: ENSP00000467452.1:p.Glu18Gln
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.50C>G
  hgvsp: ENSP00000465604.2:p.Ser17Cys
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.136G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.52G>C
  hgvsp: ENSP00000314813.4:p.Glu18Gln
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.121G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.102G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.52G>C
  hgvsp: ENSP00000464146.3:p.Glu18Gln
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13966
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
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: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29941
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2174
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu18Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

19-2269651-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269651
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269651
    reference: chr 19
allele count: 1
allele frequency: 1.748618591312863e-5
allele num: 57188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.54G>A
  hgvsp: ENST00000322297.4:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.54G>A
  hgvsp: ENST00000590943.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.54G>A
  hgvsp: ENST00000582888.4:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.104G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.123G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.54G>A
  hgvsp: ENST00000602676.2:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.54G>A
  hgvsp: ENST00000583542.4:c.54G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.48C>T
  hgvsp: ENST00000593238.2:c.48C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.138G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27108
  bin: 7.5e0
  variant carriers: 0
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: 3287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1695
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu18Glu
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD

19-2269659-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269659
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269659
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 57106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.112G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.62G>A
  hgvsp: ENSP00000473381.1:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.131G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.62G>A
  hgvsp: ENSP00000467452.1:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.40C>T
  hgvsp: ENSP00000465604.2:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.62G>A
  hgvsp: ENSP00000463955.3:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.62G>A
  hgvsp: ENSP00000314813.4:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.62G>A
  hgvsp: ENSP00000464146.3:p.Gly21Glu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.146G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4360
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26724
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29659
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly21Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

19-2269661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269661
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269661
    reference: chr 19
allele count: 1
allele frequency: 1.777777777777778e-5
allele num: 56250
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.64G>A
  hgvsp: ENSP00000473381.1:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.148G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.38C>T
  hgvsp: ENSP00000465604.2:p.Ser13Phe
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.64G>A
  hgvsp: ENSP00000464146.3:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.64G>A
  hgvsp: ENSP00000314813.4:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.64G>A
  hgvsp: ENSP00000467452.1:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.133G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.114G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.64G>A
  hgvsp: ENSP00000463955.3:p.Asp22Asn
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9897
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26493
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5037
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2415
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp22Asn
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

19-2269669-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269669
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269669
    reference: chr 19
allele count: 2
allele frequency: 3.613500036135e-5
allele num: 55348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.141C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.72C>T
  hgvsp: ENST00000590943.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.72C>T
  hgvsp: ENST00000602676.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.72C>T
  hgvsp: ENST00000583542.4:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.72C>T
  hgvsp: ENST00000322297.4:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.122C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.72C>T
  hgvsp: ENST00000582888.4:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.30G>A
  hgvsp: ENST00000593238.2:c.30G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.156C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5222
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5621
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27762
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2499
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11269
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro24Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum

19-2269679-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269679
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269679
    reference: chr 19
allele count: 1
allele frequency: 1.823420006564312e-5
allele num: 54842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.132A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.82A>G
  hgvsp: ENSP00000464146.3:p.Ile28Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.166A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.82A>G
  hgvsp: ENSP00000473381.1:p.Ile28Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.151A>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.20T>C
  hgvsp: ENSP00000465604.2:p.Met7Thr
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.82A>G
  hgvsp: ENSP00000314813.4:p.Ile28Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.82A>G
  hgvsp: ENSP00000467452.1:p.Ile28Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.82A>G
  hgvsp: ENSP00000463955.3:p.Ile28Val
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10116
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1988
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11016
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile28Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

19-2269686-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269686
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269686
    reference: chr 19
allele count: 3
allele frequency: 5.439512619669277e-5
allele num: 55152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.89C>T
  hgvsp: ENSP00000463955.3:p.Ala30Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.89C>T
  hgvsp: ENSP00000314813.4:p.Ala30Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.89C>T
  hgvsp: ENSP00000464146.3:p.Ala30Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.89C>T
  hgvsp: ENSP00000473381.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.139C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.13G>A
  hgvsp: ENSP00000465604.2:p.Ala5Thr
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.173C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.89C>T
  hgvsp: ENSP00000467452.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.158C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26441
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1840
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala30Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

19-2269692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269692
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269692
    reference: chr 19
allele count: 3
allele frequency: 5.486868095690979e-5
allele num: 54676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.145G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.95G>A
  hgvsp: ENSP00000473381.1:p.Arg32His
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.95G>A
  hgvsp: ENSP00000463955.3:p.Arg32His
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.95G>A
  hgvsp: ENSP00000467452.1:p.Arg32His
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.95G>A
  hgvsp: ENSP00000464146.3:p.Arg32His
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.7C>T
  hgvsp: ENSP00000465604.2:p.Arg3Trp
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.179G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.164G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.95G>A
  hgvsp: ENSP00000314813.4:p.Arg32His
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10974
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10322
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26482
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11647
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg32His
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum

19-2269692-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269692
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269692
    reference: chr 19
allele count: 406
allele frequency: 7.425561489501792e-3
allele num: 54676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.179G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.95G>T
  hgvsp: ENSP00000314813.4:p.Arg32Leu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.95G>T
  hgvsp: ENSP00000463955.3:p.Arg32Leu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.95G>T
  hgvsp: ENSP00000473381.1:p.Arg32Leu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.95G>T
  hgvsp: ENSP00000464146.3:p.Arg32Leu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.95G>T
  hgvsp: ENSP00000467452.1:p.Arg32Leu
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.7C>A
  hgvsp: ENST00000593238.2:c.7C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.164G>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.145G>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 2.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 2.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 1.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 26482
  bin: 7.5e0
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 10322
  bin: 1.25e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10974
  bin: 2.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1282
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2191
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 4.25e1
  variant carriers: 7
hgvs: p.Arg32Leu
num of homozygotes: 8
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

19-2269695-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269695
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269695
    reference: chr 19
allele count: 2
allele frequency: 3.647904278991719e-5
allele num: 54826
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.98C>G
  hgvsp: ENSP00000314813.4:p.Thr33Ser
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.4G>C
  hgvsp: ENSP00000465604.2:p.Val2Leu
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.98C>G
  hgvsp: ENSP00000467452.1:p.Thr33Ser
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.98C>G
  hgvsp: ENSP00000463955.3:p.Thr33Ser
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.98C>G
  hgvsp: ENSP00000464146.3:p.Thr33Ser
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.98C>G
  hgvsp: ENSP00000473381.1:p.Thr33Ser
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.182C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.167C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.148C>G
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26677
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29927
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1125
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr33Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-2269696-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269696
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269696
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 54894
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.99C>T
  hgvsp: ENST00000602676.2:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.3G>A
  hgvsp: ENSP00000465604.2:p.Met1?
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.99C>T
  hgvsp: ENST00000590943.2:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.99C>T
  hgvsp: ENST00000583542.4:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.99C>T
  hgvsp: ENST00000582888.4:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.149C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.183C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.99C>T
  hgvsp: ENST00000322297.4:c.99C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.168C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: start lost
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26694
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5302
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12219
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5616
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met1?
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-2269701-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269701
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269701
    reference: chr 19
allele count: 1
allele frequency: 1.834391165572146e-5
allele num: 54514
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.104C>G
  hgvsp: ENSP00000464146.3:p.Pro35Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.188C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.154C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.104C>G
  hgvsp: ENSP00000467452.1:p.Pro35Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.104C>G
  hgvsp: ENSP00000314813.4:p.Pro35Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.104C>G
  hgvsp: ENSP00000473381.1:p.Pro35Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-3G>C
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.104C>G
  hgvsp: ENSP00000463955.3:p.Pro35Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.173C>G
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2773
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
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: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2271
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro35Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

19-2269702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269702
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269702
    reference: chr 19
allele count: 4
allele frequency: 7.349968762632759e-5
allele num: 54422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.105G>A
  hgvsp: ENST00000590943.2:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.174G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.105G>A
  hgvsp: ENST00000582888.4:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.189G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-4C>T
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.105G>A
  hgvsp: ENST00000322297.4:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.105G>A
  hgvsp: ENST00000583542.4:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.105G>A
  hgvsp: ENST00000602676.2:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.155G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2552
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10306
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2771
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2237
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro35Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

19-2269703-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269703
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269703
    reference: chr 19
allele count: 1
allele frequency: 1.837559720690922e-5
allele num: 54420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.106C>T
  hgvsp: ENSP00000464146.3:p.Leu36Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.106C>T
  hgvsp: ENSP00000467452.1:p.Leu36Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.106C>T
  hgvsp: ENSP00000314813.4:p.Leu36Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.190C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.106C>T
  hgvsp: ENSP00000463955.3:p.Leu36Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.156C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.106C>T
  hgvsp: ENSP00000473381.1:p.Leu36Phe
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-5G>A
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.175C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26691
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu36Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

19-2269705-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269705
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269705
    reference: chr 19
allele count: 1
allele frequency: 1.837694795648339e-5
allele num: 54416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.177C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.158C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.108C>T
  hgvsp: ENST00000583542.4:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.108C>T
  hgvsp: ENST00000322297.4:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.108C>T
  hgvsp: ENST00000602676.2:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.108C>T
  hgvsp: ENST00000582888.4:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-7G>A
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.108C>T
  hgvsp: ENST00000590943.2:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.192C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1964
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu36Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

19-2269706-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269706
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269706
    reference: chr 19
allele count: 1
allele frequency: 1.834256575809824e-5
allele num: 54518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.109C>T
  hgvsp: ENST00000590943.2:c.109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.109C>T
  hgvsp: ENST00000602676.2:c.109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.109C>T
  hgvsp: ENST00000582888.4:c.109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.109C>T
  hgvsp: ENST00000322297.4:c.109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.109C>T
  hgvsp: ENST00000583542.4:c.109C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.159C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.178C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.193C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-8G>A
  variant of: http://identifiers.org/hgnc/24963
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10293
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2202
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu37Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

19-2269710-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269710
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269710
    reference: chr 19
allele count: 1
allele frequency: 1.871187455559298e-5
allele num: 53442
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.113G>C
  hgvsp: ENSP00000467452.1:p.Ser38Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.113G>C
  hgvsp: ENSP00000464146.3:p.Ser38Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.113G>C
  hgvsp: ENSP00000473381.1:p.Ser38Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.113G>C
  hgvsp: ENSP00000314813.4:p.Ser38Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.182G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.197G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.113G>C
  hgvsp: ENSP00000463955.3:p.Ser38Thr
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.163G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-12C>G
  variant of: http://identifiers.org/hgnc/24963
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10533
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5795
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6016
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2191
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29866
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser38Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/19-2269716-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269716
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269716
    reference: chr 19
allele count: 15
allele frequency: 2.853989877849233e-4
allele num: 52558
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.119A>C
  hgvsp: ENSP00000314813.4:p.His40Pro
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.119A>C
  hgvsp: ENSP00000467452.1:p.His40Pro
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.119A>C
  hgvsp: ENSP00000473381.1:p.His40Pro
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-18T>G
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.169A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.203A>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.119A>C
  hgvsp: ENSP00000464146.3:p.His40Pro
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.119A>C
  hgvsp: ENSP00000463955.3:p.His40Pro
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.188A>C
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10713
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10928
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26688
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5946
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 2.5e0
  variant carriers: 1
hgvs: p.His40Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

19-2269721-C-CGCG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269721
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269724
    reference: chr 19
allele count: 1
allele frequency: 1.908615490323319e-5
allele num: 52394
alternate allele: CGCG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.214_216dupGGC
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.130_132dupGGC
  hgvsp: ENSP00000464146.3:p.Gly44dup
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-26_-24dupCGC
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.180_182dupGGC
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.130_132dupGGC
  hgvsp: ENSP00000463955.3:p.Gly44dup
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.130_132dupGGC
  hgvsp: ENSP00000473381.1:p.Gly44dup
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.130_132dupGGC
  hgvsp: ENSP00000467452.1:p.Gly44dup
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.130_132dupGGC
  hgvsp: ENSP00000314813.4:p.Gly44dup
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.199_201dupGGC
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6370
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10902
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly44dup
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

19-2269725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269725
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269725
    reference: chr 19
allele count: 1
allele frequency: 1.945979606133728e-5
allele num: 51388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.128G>A
  hgvsp: ENSP00000314813.4:p.Gly43Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.197G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.128G>A
  hgvsp: ENSP00000473381.1:p.Gly43Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.128G>A
  hgvsp: ENSP00000464146.3:p.Gly43Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.128G>A
  hgvsp: ENSP00000467452.1:p.Gly43Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.128G>A
  hgvsp: ENSP00000463955.3:p.Gly43Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-27C>T
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.178G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.212G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26667
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly43Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

19-2269726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269726
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269726
    reference: chr 19
allele count: 2
allele frequency: 3.903505347802327e-5
allele num: 51236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.213C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.198C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.129C>T
  hgvsp: ENST00000583542.4:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.129C>T
  hgvsp: ENST00000590943.2:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-28G>A
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.179C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.129C>T
  hgvsp: ENST00000582888.4:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.129C>T
  hgvsp: ENST00000322297.4:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.129C>T
  hgvsp: ENST00000602676.2:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26626
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2002
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31362
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly43Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-2269727-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269727
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269727
    reference: chr 19
allele count: 1
allele frequency: 1.967496950379727e-5
allele num: 50826
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.130G>C
  hgvsp: ENSP00000463955.3:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.130G>C
  hgvsp: ENSP00000467452.1:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.199G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.214G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.130G>C
  hgvsp: ENSP00000314813.4:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.180G>C
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-29C>G
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.130G>C
  hgvsp: ENSP00000473381.1:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.130G>C
  hgvsp: ENSP00000464146.3:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26643
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11134
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 963
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly44Arg
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

19-2269728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269728
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269728
    reference: chr 19
allele count: 696
allele frequency: 1.361768734102915e-2
allele num: 51110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.200G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.131G>A
  hgvsp: ENSP00000463955.3:p.Gly44Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.181G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.131G>A
  hgvsp: ENSP00000464146.3:p.Gly44Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-30C>T
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.131G>A
  hgvsp: ENSP00000314813.4:p.Gly44Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.131G>A
  hgvsp: ENSP00000473381.1:p.Gly44Asp
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.215G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.131G>A
  hgvsp: ENSP00000467452.1:p.Gly44Asp
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11208
  bin: 1.25e1
  variant carriers: 325
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9689
  bin: 2.25e1
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 1.75e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26454
  bin: 7.5e0
  variant carriers: 128
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7054
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 2.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7219
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10807
  bin: 6.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 7.75e1
  variant carriers: 14
hgvs: p.Gly44Asp
num of homozygotes: 28
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

19-2269735-CAGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269735
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269732
    reference: chr 19
allele count: 1
allele frequency: 2.036411029202134e-5
allele num: 49106
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.223_225delAGT
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.139_141delAGT
  hgvsp: ENSP00000467452.1:p.Ser47del
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.139_141delAGT
  hgvsp: ENSP00000464146.3:p.Ser47del
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.139_141delAGT
  hgvsp: ENSP00000463955.3:p.Ser47del
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.208_210delAGT
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.189_191delAGT
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-40_-38delACT
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.139_141delAGT
  hgvsp: ENSP00000473381.1:p.Ser47del
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.139_141delAGT
  hgvsp: ENSP00000314813.4:p.Ser47del
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26547
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8094
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11446
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31961
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser47del
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: CAGT
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

19-2269737-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269737
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269737
    reference: chr 19
allele count: 2
allele frequency: 4.094836411285369e-5
allele num: 48842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.209G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.140G>A
  hgvsp: ENSP00000464146.3:p.Ser47Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.140G>A
  hgvsp: ENSP00000467452.1:p.Ser47Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.140G>A
  hgvsp: ENSP00000473381.1:p.Ser47Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.140G>A
  hgvsp: ENSP00000314813.4:p.Ser47Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.224G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.140G>A
  hgvsp: ENSP00000463955.3:p.Ser47Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.190G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11512
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2026
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser47Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-2269743-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269743
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269743
    reference: chr 19
allele count: 2
allele frequency: 4.244121891180715e-5
allele num: 47124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-45C>T
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146G>A
  hgvsp: ENSP00000463955.3:p.Arg49Lys
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146G>A
  hgvsp: ENSP00000473381.1:p.Ser49Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146G>A
  hgvsp: ENSP00000314813.4:p.Ser49Asn
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146G>A
  hgvsp: ENSP00000467452.1:p.Arg49Lys
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146G>A
  hgvsp: ENSP00000464146.3:p.Ser49Asn
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser49Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

19-2269750-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269750
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269750
    reference: chr 19
allele count: 4
allele frequency: 8.92140244446427e-5
allele num: 44836
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+7G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+7G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+7G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-52C>T
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+7G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+7G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+7G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+7G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+7G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25035
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12408
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
hgvs: c.146+7G>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

19-2269751-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269751
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269751
    reference: chr 19
allele count: 15
allele frequency: 3.420440552743193e-4
allele num: 43854
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+8C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+8C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+8C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+8C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+8C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+8C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-53G>A
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+8C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+8C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11995
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12603
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24642
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2486
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 6.75e1
  variant carriers: 1
hgvs: c.146+8C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-2269755-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269755
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269755
    reference: chr 19
allele count: 4
allele frequency: 9.551098376313276e-5
allele num: 41880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-57C>T
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+12G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+12G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+12G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+12G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+12G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+12G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+12G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+12G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12573
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5624
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13483
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP

19-2269756-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269756
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269756
    reference: chr 19
allele count: 1
allele frequency: 2.375409758183287e-5
allele num: 42098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+13C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+13C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+13C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+13C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-58G>A
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+13C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+13C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+13C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+13C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2283
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

19-2269757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269757
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269757
    reference: chr 19
allele count: 1
allele frequency: 2.38914373088685e-5
allele num: 41856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+14C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+14C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+14C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+14C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+14C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+14C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000167476
  ensembl protein: ENSP00000465604
  ensembl transcript: ENST00000593238
  gene symbol: JSRP1
  hgvsc: ENST00000593238.2:c.-59G>A
  variant of: http://identifiers.org/hgnc/24963
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+14C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+14C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12494
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24201
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13399
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28362
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5744
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

19-2269763-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269763
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269763
    reference: chr 19
allele count: 1
allele frequency: 2.49925022493252e-5
allele num: 40012
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+20C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+20C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+20C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+20C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+20C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+20C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+20C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+20C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12433
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23209
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16011
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26964
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1792
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

19-2269765-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269765
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269765
    reference: chr 19
allele count: 1
allele frequency: 2.738675576491209e-5
allele num: 36514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+22G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+22G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+22G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+22G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+22G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+22G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+22G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+22G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22303
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum

19-2269781-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269781
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269781
    reference: chr 19
allele count: 1
allele frequency: 3.261365860022177e-5
allele num: 30662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+38C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+38C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9502
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22770
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18935
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 2.75e1
  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: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16764
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

19-2269782-CGGCCGCGCA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269782
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269773
    reference: chr 19
allele count: 3
allele frequency: 9.960820771631583e-5
allele num: 30118
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 22966
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9260
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2152
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20313
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: CGGCCGCGCA
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

19-2269783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269783
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269783
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 27916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+40G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+40G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+40G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+40G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+40G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+40G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+40G>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+40G>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 18920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23623
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  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: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6383
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2768
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19898
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2175
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1757
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

19-2269785-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269785
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269785
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 28022
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+42C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+42C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+42C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+42C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+42C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+42C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+42C>G
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+42C>G
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23693
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19019
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6365
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20161
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/19-2269786-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269786
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269786
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 28100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+43C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+43C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+43C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+43C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+43C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+43C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+43C>A
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+43C>A
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23681
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19048
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20255
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

19-2269786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 2269786
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 2269786
    reference: chr 19
allele count: 0
allele frequency: 0.0e0
allele num: 28100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000592787
  gene symbol: OAZ1
  hgvsc: ENST00000592787.2:n.230+43C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000467452
  ensembl transcript: ENST00000590943
  gene symbol: OAZ1
  hgvsc: ENST00000590943.2:c.146+43C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000581150
  gene symbol: OAZ1
  hgvsc: ENST00000581150.2:n.215+43C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000314813
  ensembl transcript: ENST00000322297
  gene symbol: OAZ1
  hgvsc: ENST00000322297.4:c.146+43C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000464146
  ensembl transcript: ENST00000583542
  gene symbol: OAZ1
  hgvsc: ENST00000583542.4:c.146+43C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl transcript: ENST00000593012
  gene symbol: OAZ1
  hgvsc: ENST00000593012.1:n.196+43C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000463955
  ensembl transcript: ENST00000582888
  gene symbol: OAZ1
  hgvsc: ENST00000582888.4:c.146+43C>T
  variant of: http://identifiers.org/hgnc/8095
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104904
  ensembl protein: ENSP00000473381
  ensembl transcript: ENST00000602676
  gene symbol: OAZ1
  hgvsc: ENST00000602676.2:c.146+43C>T
  variant of: http://identifiers.org/hgnc/8095
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19048
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23681
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20255
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1836
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 19590
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2449
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27410
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1676
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1848
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.659574468085106e-3
allele num: 376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.175e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.11929e5

VQSLOD
type: SiteQuality
SIO_000300: -7.725e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.23e0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1676
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19590
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1848
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.11929e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -7.725e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.175e-1

QD
type: SiteQuality
SIO_000300: 9.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeQuality
all individuals: 708
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1525
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23571
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.00160128102482e-4
allele num: 4996
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.501e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 3.40746e5

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.065e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 26
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25232
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23571
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 8.237232289950577e-4
allele num: 1214
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.501e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.065e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

DP
type: SiteQuality
SIO_000300: 3.40746e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeQuality
all individuals: 23
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 83
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 775
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 912
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 925
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 285
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 87
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 42
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 3

South Asian
type: Population
allele count: 4
allele frequency: 1.616814874696847e-3
allele num: 2474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.632568634825122e-3
allele num: 5318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

FS
type: SiteQuality
SIO_000300: 4.821e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.67e-2

QD
type: SiteQuality
SIO_000300: 1.037e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 3.47379e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -3.949e-1

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23704
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25314
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.650967506389193e-4
allele num: 5478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.324e1

DP
type: SiteQuality
SIO_000300: 3.56413e5

VQSLOD
type: SiteQuality
SIO_000300: -1.005e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.73e-2

FS
type: SiteQuality
SIO_000300: 7.048e0

MQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.96e-1

GenotypeQuality
all individuals: 956
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23133
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.755001755001755e-4
allele num: 5698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2710
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.62195e5

QD
type: SiteQuality
SIO_000300: 8.26e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.314e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.52e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.251e0

GenotypeQuality
all individuals: 308
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2506
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 918
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.442340791738382e-4
allele num: 5810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

QD
type: SiteQuality
SIO_000300: 1.112e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.54e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.69625e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26958
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5810
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 7.692307692307692e-4
allele num: 1300
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.112e1

DP
type: SiteQuality
SIO_000300: 3.69625e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.54e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

GenotypeQuality
all individuals: 882
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1478
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2675
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.399048266485384e-4
allele num: 2942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.76658e5

BaseQRankSum
type: SiteQuality
SIO_000300: -8.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.83e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.453e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

QD
type: SiteQuality
SIO_000300: 6.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.26e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1403
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3024
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.838235294117647e-3
allele num: 544
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.98e-1

DP
type: SiteQuality
SIO_000300: 3.82146e5

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

FS
type: SiteQuality
SIO_000300: 4.192e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.14e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.97e-2

QD
type: SiteQuality
SIO_000300: 1.09e1

GenotypeQuality
all individuals: 725
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3128
num of homozygotes: 0

Latino
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: 560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.3e0

QD
type: SiteQuality
SIO_000300: 1.232e1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.33e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 3.90236e5

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20585
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 89
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 96
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.19693094629156e-4
allele num: 3128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.592356687898089e-4
allele num: 6280
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.90236e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

QD
type: SiteQuality
SIO_000300: 1.232e1

VQSLOD
type: SiteQuality
SIO_000300: 4.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 799
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29896
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1393
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 106
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1464
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 1.005e1

DP
type: SiteQuality
SIO_000300: 4.06331e5

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.81e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.645e0

GenotypeQuality
all individuals: 1220
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 385
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18331
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 961
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3910
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.40686550365785e-4
allele num: 7108
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

DP
type: SiteQuality
SIO_000300: 4.16254e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.94e-2

FS
type: SiteQuality
SIO_000300: 1.158e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.19e0

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

GenotypeQuality
all individuals: 739
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18331
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 90
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3645
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3910
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7108
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.16254e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.94e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.582e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 7.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 1.158e0

GenotypeQuality
all individuals: 125
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 469
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17629
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31422
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7334
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.861e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

QD
type: SiteQuality
SIO_000300: 1.065e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.431e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.53e-2

DP
type: SiteQuality
SIO_000300: 4.24126e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 407
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 59
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 31711
bin: 2.25e1
variant carriers: 4

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1102
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.25e1
variant carriers: 7

GenotypeQuality
all individuals: 100
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 9.75e1
variant carriers: 81

GenotypeQuality
all individuals: 450
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3998
bin: 6.25e1
variant carriers: 2

Latino
type: Population
allele count: 2
allele frequency: 2.840909090909091e-3
allele num: 704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 81
allele frequency: 1.055512118842846e-2
allele num: 7674
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.389999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.451e0

QD
type: SiteQuality
SIO_000300: 1.162e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

DP
type: SiteQuality
SIO_000300: 4.35333e5

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 450
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16773
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 407
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3998
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.606202762574928e-4
allele num: 7674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4260
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1556
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.389999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

FS
type: SiteQuality
SIO_000300: 1.451e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

DP
type: SiteQuality
SIO_000300: 4.35333e5

QD
type: SiteQuality
SIO_000300: 1.162e1

GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4504
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32607
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1618
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -9.688e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.66e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.46556e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 15889
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 138
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4642
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.688e-1

DP
type: SiteQuality
SIO_000300: 4.46556e5

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.66e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

GenotypeQuality
all individuals: 14043
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32749
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1191
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1049
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4875
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.100594320933304e-4
allele num: 9086
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1030
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.08e0

DP
type: SiteQuality
SIO_000300: 4.68351e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.86e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 231
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6029
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 701
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11830
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1440
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 198
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1407
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 3.664345914254306e-4
allele num: 10916
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.466e0

DP
type: SiteQuality
SIO_000300: 5.02709e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.45e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.85e-1

QD
type: SiteQuality
SIO_000300: 7.03e0

GenotypeQuality
all individuals: 252
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8698
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 439
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7098
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2320
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.431024613623354e-4
allele num: 6988
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.79e-1

DP
type: SiteQuality
SIO_000300: 5.57651e5

FS
type: SiteQuality
SIO_000300: 2.632e0

QD
type: SiteQuality
SIO_000300: 7.34e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.459e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.517e0

GenotypeQuality
all individuals: 9355
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6957
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 35045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 792
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1920
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7872
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1282
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

MQ
type: SiteQuality
SIO_000300: 5.805e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.049e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 2.79e0

DP
type: SiteQuality
SIO_000300: 5.98791e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

QD
type: SiteQuality
SIO_000300: 7.65e0

GenotypeQuality
all individuals: 700
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9355
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6957
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1513
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1920
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 5.98791e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.05e-1

FS
type: SiteQuality
SIO_000300: 2.79e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQ
type: SiteQuality
SIO_000300: 5.805e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.049e0

QD
type: SiteQuality
SIO_000300: 7.65e0

GenotypeQuality
all individuals: 1412
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32169
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3735
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 227
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1930
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.801703163017032e-5
allele num: 26304
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.65e-1

FS
type: SiteQuality
SIO_000300: 2.363e0

QD
type: SiteQuality
SIO_000300: 1.22e1

VQSLOD
type: SiteQuality
SIO_000300: -2.17e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

DP
type: SiteQuality
SIO_000300: 7.27216e5

GenotypeQuality
all individuals: 1478
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31363
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 389
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.589890867317634e-5
allele num: 27856
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

DP
type: SiteQuality
SIO_000300: 7.47422e5

QD
type: SiteQuality
SIO_000300: 1.214e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

GenotypeQuality
all individuals: 262
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1130
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31188
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1487
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1136
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 374
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3424
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.976190476190476e-4
allele num: 3360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3708
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2016
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.015e1

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.2e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.98e0

DP
type: SiteQuality
SIO_000300: 7.50642e5

FS
type: SiteQuality
SIO_000300: 1.829e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

GenotypeQuality
all individuals: 1774
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 808
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30041
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15659
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31724
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.689922480620155e-5
allele num: 10320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4168
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.0138e1

MQRankSum
type: SiteQuality
SIO_000300: 7.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 7.71734e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.012e0

QD
type: SiteQuality
SIO_000300: 6.96e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.723e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1364
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3438
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 604
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15377
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.14149283739633e-5
allele num: 31832
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4050
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2296
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.299999999999999e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.398e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

QD
type: SiteQuality
SIO_000300: 3.98e0

VQSLOD
type: SiteQuality
SIO_000300: -3.161e0

DP
type: SiteQuality
SIO_000300: 7.7053e5

GenotypeQuality
all individuals: 1215
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1357
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3864
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 418
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3750
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.352941176470588e-4
allele num: 4250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.6411e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.03e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.862e0

VQSLOD
type: SiteQuality
SIO_000300: -3.778e0

FS
type: SiteQuality
SIO_000300: 1.685e0

MQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.75e-1

QD
type: SiteQuality
SIO_000300: 7.53e0

GenotypeQuality
all individuals: 559
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13750
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4074
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29528
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3708
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4240
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.121878121878122e-5
allele num: 32032
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.793e0

VQSLOD
type: SiteQuality
SIO_000300: -2.855e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

DP
type: SiteQuality
SIO_000300: 7.59312e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.423e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.05e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.793e0

FS
type: SiteQuality
SIO_000300: 2.218e0

QD
type: SiteQuality
SIO_000300: 1.752e1

GenotypeQuality
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1119
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2363
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4650
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13749
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4226
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32034
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.26e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.17e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 7.47993e5

FS
type: SiteQuality
SIO_000300: 7.203e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1472
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2362
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2083
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28512
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 393
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1131
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2216
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3968
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.779321845469705e-4
allele num: 3598
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.268e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.012e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 5.811e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.59e0

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

DP
type: SiteQuality
SIO_000300: 7.37245e5

GenotypeQuality
all individuals: 513
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1582
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2575
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10246
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.883506343713956e-4
allele num: 3468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.568053415511043e-4
allele num: 3894
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31166
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.113e0

MQRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.919e0

DP
type: SiteQuality
SIO_000300: 7.20906e5

QD
type: SiteQuality
SIO_000300: 2.096e1

FS
type: SiteQuality
SIO_000300: 1.952e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

GenotypeQuality
all individuals: 520
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27367
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2582
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 852
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5897
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2539
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2014
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.525252525252525e-3
allele num: 396
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3818
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30932
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.42e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.07e0

VQSLOD
type: SiteQuality
SIO_000300: -4.359e-1

FS
type: SiteQuality
SIO_000300: 2.522e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 7.12402e5

BaseQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

GenotypeQuality
all individuals: 474
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11369
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28967
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5788
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1151
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 199
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2413
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1986
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 7.720020586721565e-4
allele num: 3886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31146
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

QD
type: SiteQuality
SIO_000300: 8.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

FS
type: SiteQuality
SIO_000300: 1.4508e1

DP
type: SiteQuality
SIO_000300: 7.21863e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.983e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2312
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29266
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5664
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3482
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 9.773897178601681e-5
allele num: 30694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3856
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1942
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.432e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.37e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.30262e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

GenotypeQuality
all individuals: 5664
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 589
bin: 5.25e1
variant carriers: 12

GenotypeQuality
all individuals: 11647
bin: 6.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1728
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 97
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 2312
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 632
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1056
bin: 6.75e1
variant carriers: 11

GenotypeQuality
all individuals: 29266
bin: 2.25e1
variant carriers: 14

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 17

GenotypeQuality
all individuals: 39
bin: 9.25e1
variant carriers: 12

GenotypeQuality
all individuals: 163
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 638
bin: 4.75e1
variant carriers: 8

GenotypeQuality
all individuals: 177
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 413
bin: 9.75e1
variant carriers: 380

GenotypeQuality
all individuals: 211
bin: 5.75e1
variant carriers: 11

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1942
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

Latino
type: Population
allele count: 22
allele frequency: 5.705394190871369e-3
allele num: 3856
num of homozygotes: 0

African
type: Population
allele count: 372
allele frequency: 8.912314326784859e-2
allele num: 4174
num of homozygotes: 8

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 3.25796572620056e-4
allele num: 30694
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.973554371422933e-4
allele num: 10134
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.37e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 7.30262e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

QD
type: SiteQuality
SIO_000300: 1.432e1

GenotypeQuality
all individuals: 5623
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 184
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11938
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2187
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 357
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4026
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.861932938856015e-5
allele num: 10140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.232688950669167e-5
allele num: 30934
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.234e1

FS
type: SiteQuality
SIO_000300: 6.138e0

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.871e1

DP
type: SiteQuality
SIO_000300: 7.23616e5

VQSLOD
type: SiteQuality
SIO_000300: -5.579e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

GenotypeQuality
all individuals: 1104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30968
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1926
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3940
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4026
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.104e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.2466e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.39e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e0

GenotypeQuality
all individuals: 336
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29972
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11886
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5739
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2062
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.252667187093417e-5
allele num: 30744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1910
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.73e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.023e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.44e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.666e-1

DP
type: SiteQuality
SIO_000300: 7.21951e5

MQRankSum
type: SiteQuality
SIO_000300: -4.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

GenotypeQuality
all individuals: 2013
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 12198
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5741
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30303
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1906
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 8.561643835616438e-4
allele num: 3504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.262855651265988e-5
allele num: 30648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.286e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.46e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

DP
type: SiteQuality
SIO_000300: 7.23418e5

GenotypeQuality
all individuals: 30201
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1013
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5757
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11982
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2248
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 553
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3920
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.265626020508131e-5
allele num: 30622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1904
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-1

FS
type: SiteQuality
SIO_000300: 1.303e1

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

QD
type: SiteQuality
SIO_000300: 9.5e0

DP
type: SiteQuality
SIO_000300: 7.2052e5

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.706e0

GenotypeQuality
all individuals: 30463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12312
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1042
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5778
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1536
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3942
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3922
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.854158454867954e-5
allele num: 10148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3476
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.083e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.099e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.32e-1

DP
type: SiteQuality
SIO_000300: 7.21216e5

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.61e-1

GenotypeQuality
all individuals: 446
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5770
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1925
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10142
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1896
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3936
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3950
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.857142857142857e-4
allele num: 3500
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.177e0

MQ
type: SiteQuality
SIO_000300: 5.833e1

QD
type: SiteQuality
SIO_000300: 7.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

FS
type: SiteQuality
SIO_000300: 2.363e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.94e-1

DP
type: SiteQuality
SIO_000300: 7.22828e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.097e0

GenotypeQuality
all individuals: 158
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 455
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11489
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1907
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1086
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 992
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.34001336005344e-5
allele num: 29940
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10108
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.13506e5

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 6.154e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.45e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 7.54e0

GenotypeQuality
all individuals: 151
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1759
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2080
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 854
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 11638
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1823
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30380
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 950
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 51
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 403
bin: 4.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 2.385171050838217e-4
allele num: 29348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3870
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3438
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 2.168021680216802e-3
allele num: 3690
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.81e1

MQ
type: SiteQuality
SIO_000300: 5.79e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.727e0

FS
type: SiteQuality
SIO_000300: 5.7279e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.57e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

DP
type: SiteQuality
SIO_000300: 7.11929e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.707e0

GenotypeQuality
all individuals: 1737
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 482
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11459
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31246
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6537
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1666
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.963841138114997e-4
allele num: 3374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.804e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.56e-2

QD
type: SiteQuality
SIO_000300: 1.264e1

DP
type: SiteQuality
SIO_000300: 7.02536e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.524e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.204e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

FS
type: SiteQuality
SIO_000300: 2.246e0

GenotypeQuality
all individuals: 1947
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7035
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 937
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2038
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10833
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 189
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.493815945775976e-5
allele num: 28622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.36e-1

FS
type: SiteQuality
SIO_000300: 1.64e0

DP
type: SiteQuality
SIO_000300: 6.89591e5

VQSLOD
type: SiteQuality
SIO_000300: -1.273e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.66e-2

QD
type: SiteQuality
SIO_000300: 5.94e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

GenotypeQuality
all individuals: 341
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11027
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7059
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1617
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1720
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.712967986977754e-4
allele num: 3686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3720
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.503117774819589e-5
allele num: 28546
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

DP
type: SiteQuality
SIO_000300: 6.9061e5

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

QD
type: SiteQuality
SIO_000300: 1.039e1

FS
type: SiteQuality
SIO_000300: 2.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.29e-1

GenotypeQuality
all individuals: 1620
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7252
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 31316
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10637
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1846
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2013
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9850
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.530325496010732e-5
allele num: 28326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3646
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.849e5

BaseQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

QD
type: SiteQuality
SIO_000300: 1.489e1

GenotypeQuality
all individuals: 31206
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 639
bin: 9.75e1
variant carriers: 585

GenotypeQuality
all individuals: 362
bin: 5.25e1
variant carriers: 15

GenotypeQuality
all individuals: 668
bin: 3.75e1
variant carriers: 13

GenotypeQuality
all individuals: 592
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 25

GenotypeQuality
all individuals: 1926
bin: 2.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1510
bin: 3.25e1
variant carriers: 12

GenotypeQuality
all individuals: 185
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1535
bin: 1.75e1
variant carriers: 5

GenotypeQuality
all individuals: 284
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 207
bin: 4.25e1
variant carriers: 5

GenotypeQuality
all individuals: 213
bin: 5.75e1
variant carriers: 15

GenotypeQuality
all individuals: 35
bin: 8.75e1
variant carriers: 22

GenotypeQuality
all individuals: 101
bin: 8.25e1
variant carriers: 23

GenotypeQuality
all individuals: 978
bin: 6.75e1
variant carriers: 21

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 2.830656004529049e-4
allele num: 28262
num of homozygotes: 0

East Asian
type: Population
allele count: 74
allele frequency: 2.253349573690621e-2
allele num: 3284
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 8.116883116883117e-4
allele num: 3696
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 1.08695652173913e-2
allele num: 368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1678
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

Latino
type: Population
allele count: 607
allele frequency: 1.525125628140704e-1
allele num: 3980
num of homozygotes: 28

VQSLOD
type: SiteQuality
SIO_000300: 4.44e0

QD
type: SiteQuality
SIO_000300: 1.351e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.139e0

FS
type: SiteQuality
SIO_000300: 5.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.88637e5

GenotypeQuality
all individuals: 10016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 605
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8216
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3590
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.174603174603175e-4
allele num: 3150
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.468e0

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.82e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.009e1

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.25e-1

MQ
type: SiteQuality
SIO_000300: 5.887e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.25e-1

DP
type: SiteQuality
SIO_000300: 6.63308e5

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32204
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8536
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.667571334262452e-5
allele num: 27266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.435006435006435e-4
allele num: 1554
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3586
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.86e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.087e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.967e1

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

DP
type: SiteQuality
SIO_000300: 6.58062e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
all individuals: 590
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10079
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31387
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1557
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8737
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2161
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 157
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2964
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3444
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.088554720133667e-4
allele num: 9576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1450
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

DP
type: SiteQuality
SIO_000300: 6.30035e5

VQSLOD
type: SiteQuality
SIO_000300: 7.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.08e-2

QD
type: SiteQuality
SIO_000300: 1.404e1

FS
type: SiteQuality
SIO_000300: 5.007e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.27e-1

GenotypeQuality
all individuals: 138
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11628
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29818
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1689
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 646
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 1.608751608751609e-4
allele num: 24864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3248
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2888
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.33e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

FS
type: SiteQuality
SIO_000300: 9.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 5.97649e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.752e0

QD
type: SiteQuality
SIO_000300: 1.059e1

GenotypeQuality
all individuals: 137
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12339
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 741
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28815
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1628
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 71
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1765
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6366
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2339
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 9.75e1
variant carriers: 16

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24294
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9266
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1314
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 4.413619167717529e-3
allele num: 3172
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.579098067287044e-4
allele num: 2794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2690
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.47e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.271e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

DP
type: SiteQuality
SIO_000300: 5.8643e5

QD
type: SiteQuality
SIO_000300: 1.266e1

VQSLOD
type: SiteQuality
SIO_000300: 5.65e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

GenotypeQuality
all individuals: 305
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2802
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27706
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1807
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 651
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2282
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2552
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 1.328021248339973e-3
allele num: 3012
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23152
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9052
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

FS
type: SiteQuality
SIO_000300: 2.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e-1

QD
type: SiteQuality
SIO_000300: 9.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.77e-2

DP
type: SiteQuality
SIO_000300: 5.67828e5

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2335
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1714
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28379
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5814
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13600
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1752
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 617
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9070
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3028
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 8.19672131147541e-4
allele num: 1220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23308
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.52e-1

DP
type: SiteQuality
SIO_000300: 5.66777e5

MQ
type: SiteQuality
SIO_000300: 5.875e1

FS
type: SiteQuality
SIO_000300: 2.447e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.678e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.69e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.37e-1

QD
type: SiteQuality
SIO_000300: 6.09e0

VQSLOD
type: SiteQuality
SIO_000300: -2.485e0

GenotypeQuality
all individuals: 1729
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13926
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1770
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9050
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.314808422506041e-5
allele num: 23176
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.73e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.86e-1

DP
type: SiteQuality
SIO_000300: 5.63148e5

BaseQRankSum
type: SiteQuality
SIO_000300: 6.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 2.046e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

GenotypeQuality
all individuals: 63
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2395
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22080
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 4.299226139294927e-4
allele num: 2326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.55e-1

QD
type: SiteQuality
SIO_000300: 1.12e1

VQSLOD
type: SiteQuality
SIO_000300: -1.404e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.04e-2

MQ
type: SiteQuality
SIO_000300: 5.836e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 5.35581e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.377e0

MQRankSum
type: SiteQuality
SIO_000300: 8.71e-1

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1880
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17831
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1352
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 978
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.916420845624386e-4
allele num: 2034
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20088
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.58e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.379e0

MQ
type: SiteQuality
SIO_000300: 5.763e1

DP
type: SiteQuality
SIO_000300: 5.04138e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.44e0

FS
type: SiteQuality
SIO_000300: 5.119e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.059e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3657
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5495
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20282
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2257
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2271
bin: 6.25e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2098
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 7.08215297450425e-4
allele num: 1412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16642
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8106
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.214e0

VQSLOD
type: SiteQuality
SIO_000300: -5.073e-1

DP
type: SiteQuality
SIO_000300: 4.46331e5

FS
type: SiteQuality
SIO_000300: 5.815e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.12e-2

GenotypeQuality
all individuals: 5727
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3852
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.12369871402327e-5
allele num: 16330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2062
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 1.461988304093567e-3
allele num: 1368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 234
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.366e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.18e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.852e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.51e-1

DP
type: SiteQuality
SIO_000300: 4.43344e5

QD
type: SiteQuality
SIO_000300: 5.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.1e-1

GenotypeQuality
all individuals: 433
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13501
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5458
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14864
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.684e-1

DP
type: SiteQuality
SIO_000300: 4.35355e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 1.032e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.41e-2

GenotypeQuality
all individuals: 25
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4911
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14126
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1225
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 89
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14990
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 220
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1216
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

QD
type: SiteQuality
SIO_000300: 1.265e1

MQ
type: SiteQuality
SIO_000300: 5.604e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.399e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.33e-2

DP
type: SiteQuality
SIO_000300: 4.34321e5

GenotypeQuality
all individuals: 4594
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6347
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2442
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1836
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15032
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1944
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.34213e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.74e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

QD
type: SiteQuality
SIO_000300: 1.102e1