22-50312404-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312404
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312404
    reference: chr 22
allele count: 2
allele frequency: 4.545454545454546e-2
allele num: 44
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.-11-3C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.24C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19838
  bin: 2.5e0
  variant carriers: 15
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: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2913
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16771
  bin: 7.5e0
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 3
hgvs: c.-11-3C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-50312407-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312407
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312407
    reference: chr 22
allele count: 1
allele frequency: 1.923076923076923e-2
allele num: 52
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.-11C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.-11C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.-11C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.-11C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.27C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.-11C>G
  variant of: http://identifiers.org/hgnc/28150
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  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: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20081
  bin: 2.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  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: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2852
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
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  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17083
  bin: 7.5e0
  variant carriers: 8
hgvs: c.-11C>G
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

22-50312428-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312428
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312428
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 162
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.11C>G
  hgvsp: ENSP00000384111.3:p.Pro4Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.11C>G
  hgvsp: ENSP00000386034.3:p.Pro4Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.11C>G
  hgvsp: ENSP00000332223.4:p.Pro4Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.11C>G
  hgvsp: ENSP00000383938.3:p.Pro4Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.11C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.48C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.11C>G
  hgvsp: ENSP00000387769.1:p.Pro4Arg
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 1.25e1
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2403
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro4Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

22-50312454-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312454
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312454
    reference: chr 22
allele count: 2
allele frequency: 5.813953488372093e-3
allele num: 344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.37C>T
  hgvsp: ENSP00000386034.3:p.Pro13Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.37C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.37C>T
  hgvsp: ENSP00000387769.1:p.Pro13Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.37C>T
  hgvsp: ENSP00000332223.4:p.Pro13Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.74C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.37C>T
  hgvsp: ENSP00000384111.3:p.Pro13Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.37C>T
  hgvsp: ENSP00000383938.3:p.Pro13Ser
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 23114
  bin: 2.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.25e1
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21961
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro13Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

22-50312456-GCTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312456
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312453
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.42_44delTCT
  hgvsp: ENSP00000387769.1:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.42_44delTCT
  hgvsp: ENSP00000332223.4:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.42_44delTCT
  hgvsp: ENSP00000384111.3:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.42_44delTCT
  hgvsp: ENSP00000383938.3:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.42_44delTCT
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.42_44delTCT
  hgvsp: ENSP00000386034.3:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.79_81delTCT
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu18del
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: GCTT
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

22-50312459-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312459
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312459
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.42T>G
  hgvsp: ENST00000403427.3:c.42T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.79T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.42T>G
  hgvsp: ENST00000450207.1:c.42T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.42T>G
  hgvsp: ENST00000404488.3:c.42T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.42T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.42T>G
  hgvsp: ENST00000407217.3:c.42T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.42T>G
  hgvsp: ENST00000328268.4:c.42T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22659
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 7.5e0
  variant carriers: 2
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: 23
  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: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21573
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Leu14Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

22-50312459-TCTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312459
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312456
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.90_92delTGC
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.53_55delTGC
  hgvsp: ENSP00000384111.3:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.53_55delTGC
  hgvsp: ENSP00000332223.4:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.53_55delTGC
  hgvsp: ENSP00000383938.3:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.53_55delTGC
  hgvsp: ENSP00000387769.1:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.53_55delTGC
  hgvsp: ENSP00000386034.3:p.Leu18del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.53_55delTGC
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22659
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu18del
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: TCTG
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

22-50312483-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312483
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312483
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.66G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.66G>A
  hgvsp: ENST00000403427.3:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.66G>A
  hgvsp: ENST00000404488.3:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.66G>A
  hgvsp: ENST00000328268.4:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.66G>A
  hgvsp: ENST00000407217.3:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.66G>A
  hgvsp: ENST00000450207.1:c.66G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.103G>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 20039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2366
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17804
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro22Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

22-50312543-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312543
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312543
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 30
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.126C>T
  hgvsp: ENST00000450207.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.126C>T
  hgvsp: ENST00000328268.4:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.163C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.126C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.126C>T
  hgvsp: ENST00000407217.3:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.126C>T
  hgvsp: ENST00000403427.3:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.126C>T
  hgvsp: ENST00000404488.3:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18612
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
hgvs: p.Asn42Asn
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

22-50312548-T-TTTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312548
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312551
    reference: chr 22
allele count: 4
allele frequency: 1.111111111111111e-1
allele num: 36
alternate allele: TTTC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.166+2_166+3insTTC
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.129+2_129+3insTTC
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.129+2_129+3insTTC
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.129+2_129+3insTTC
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.129+2_129+3insTTC
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.129+2_129+3insTTC
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.129+2_129+3insTTC
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18406
  bin: 2.5e0
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15970
  bin: 7.5e0
  variant carriers: 37
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
hgvs: c.129+2_129+3insTTC
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

22-50312827-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312827
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312827
    reference: chr 22
allele count: 1
allele frequency: 8.394754957102802e-6
allele num: 119122
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-51C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-51C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-51C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-51C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-51C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-51C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-51C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12769
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1870
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7952
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3736
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16201
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

22-50312834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312834
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312834
    reference: chr 22
allele count: 7
allele frequency: 5.857446488042442e-5
allele num: 119506
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-44C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-44C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-44C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-44C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-44C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-44C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-44C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1846
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5968
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3728
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8052
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2853
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

22-50312836-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312836
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312836
    reference: chr 22
allele count: 2
allele frequency: 1.672100994900092e-5
allele num: 119610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-42G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-42G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-42G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-42G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-42G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-42G>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1942
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2881
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16237
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

22-50312837-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312837
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312837
    reference: chr 22
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-41G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-41G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-41G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-41G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-41G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-41G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-41G>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16609
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3766
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

22-50312837-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312837
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312837
    reference: chr 22
allele count: 1
allele frequency: 8.358548287333457e-6
allele num: 119638
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-41G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-41G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-41G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-41G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-41G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-41G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-41G>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12871
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5965
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2884
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16237
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2880
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1387
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

22-50312838-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312838
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312838
    reference: chr 22
allele count: 6
allele frequency: 5.016554630279924e-5
allele num: 119604
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-40T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-40T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-40T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-40T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-40T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-40T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-40T>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20342
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8138
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-50312847-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312847
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312847
    reference: chr 22
allele count: 10
allele frequency: 8.343763037129746e-5
allele num: 119850
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-31A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-31A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-31A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-31A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-31A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-31A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-31A>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16961
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12963
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3825
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8280
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

22-50312847-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312847
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312847
    reference: chr 22
allele count: 1
allele frequency: 8.343763037129745e-6
allele num: 119850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-31A>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-31A>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-31A>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-31A>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-31A>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-31A>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-31A>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16250
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

22-50312850-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312850
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312850
    reference: chr 22
allele count: 1
allele frequency: 8.340422692622062e-6
allele num: 119898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-28A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-28A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-28A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-28A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-28A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-28A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-28A>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8314
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2926
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21241
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1963
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/22-50312857-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312857
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312857
    reference: chr 22
allele count: 81
allele frequency: 6.748762726833414e-4
allele num: 120022
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-21A>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-21A>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-21A>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-21A>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-21A>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-21A>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-21A>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2238
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17174
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13046
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4026
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2936
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3872
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

22-50312861-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312861
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312861
    reference: chr 22
allele count: 3
allele frequency: 2.498084801652067e-5
allele num: 120092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-17G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-17G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-17G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-17G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-17G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-17G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-17G>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2901
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4033
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8375
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21571
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

22-50312862-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312862
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312862
    reference: chr 22
allele count: 1
allele frequency: 8.326533331112925e-6
allele num: 120098
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-16C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13097
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4035
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8380
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2976
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16244
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

22-50312864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312864
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312864
    reference: chr 22
allele count: 1
allele frequency: 8.321129010784183e-6
allele num: 120176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-14C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4034
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2960
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3893
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

22-50312869-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312869
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312869
    reference: chr 22
allele count: 13967
allele frequency: 1.160782553771484e-1
allele num: 120324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-9T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-9T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-9T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-9T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-9T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-9T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-9T>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 2.25e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 4.75e1
  variant carriers: 502
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 8.25e1
  variant carriers: 725
genotype depth: GenotypeDepth
  all individuals: 5063
  bin: 9.75e1
  variant carriers: 4893
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 9.25e1
  variant carriers: 632
genotype depth: GenotypeDepth
  all individuals: 12440
  bin: 3.25e1
  variant carriers: 295
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 6.25e1
  variant carriers: 669
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 3.75e1
  variant carriers: 372
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 5.75e1
  variant carriers: 611
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 7.25e1
  variant carriers: 700
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 4.25e1
  variant carriers: 464
genotype depth: GenotypeDepth
  all individuals: 16499
  bin: 2.75e1
  variant carriers: 220
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 7.75e1
  variant carriers: 698
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 6.75e1
  variant carriers: 741
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.25e1
  variant carriers: 571
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 8.75e1
  variant carriers: 677
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 9.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 2.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 8.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 3461
  bin: 7.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 2516
  bin: 8.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 3
num of homozygotes: 911
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

22-50312870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312870
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312870
    reference: chr 22
allele count: 1
allele frequency: 8.310479514667997e-6
allele num: 120330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-8C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-8C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-8C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-8C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-8C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-8C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-8C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12859
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 9.25e1
  variant carriers: 0
hgvs: c.130-8C>T
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

22-50312876-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312876
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312876
    reference: chr 22
allele count: 1
allele frequency: 8.30675172780436e-6
allele num: 120384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130-2A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130-2A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130-2A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130-2A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167-2A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130-2A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130-2A>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9007
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12858
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4393
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3223
  bin: 7.25e1
  variant carriers: 0
hgvs: c.130-2A>G
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

22-50312878-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312878
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312878
    reference: chr 22
allele count: 1
allele frequency: 8.304544246611745e-6
allele num: 120416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.167G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.130G>A
  hgvsp: ENSP00000383938.3:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.130G>A
  hgvsp: ENSP00000384111.3:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.130G>A
  hgvsp: ENSP00000332223.4:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.130G>A
  hgvsp: ENSP00000386034.3:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.130G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.130G>A
  hgvsp: ENSP00000387769.1:p.Gly44Arg
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2462
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly44Arg
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

22-50312888-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312888
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312888
    reference: chr 22
allele count: 2
allele frequency: 1.66021948101539e-5
allele num: 120466
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.140A>G
  hgvsp: ENSP00000383938.3:p.Asp47Gly
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.140A>G
  hgvsp: ENSP00000387769.1:p.Asp47Gly
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.177A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.140A>G
  hgvsp: ENSP00000384111.3:p.Asp47Gly
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.140A>G
  hgvsp: ENSP00000332223.4:p.Asp47Gly
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.140A>G
  hgvsp: ENSP00000386034.3:p.Asp47Gly
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.140A>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3447
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp47Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

22-50312895-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312895
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312892
    reference: chr 22
allele count: 2
allele frequency: 1.659723490066555e-5
allele num: 120502
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.153_155delGAA
  hgvsp: ENSP00000383938.3:p.Lys51del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.153_155delGAA
  hgvsp: ENSP00000386034.3:p.Lys51del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.153_155delGAA
  hgvsp: ENSP00000332223.4:p.Lys51del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.190_192delGAA
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.153_155delGAA
  hgvsp: ENSP00000387769.1:p.Lys51del
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.153_155delGAA
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.153_155delGAA
  hgvsp: ENSP00000384111.3:p.Lys51del
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3446
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9007
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys51del
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: AAAG
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

22-50312901-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312901
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312901
    reference: chr 22
allele count: 1
allele frequency: 8.299719469481931e-6
allele num: 120486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.153G>A
  hgvsp: ENST00000403427.3:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.153G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.153G>A
  hgvsp: ENST00000404488.3:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.153G>A
  hgvsp: ENST00000450207.1:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.153G>A
  hgvsp: ENST00000407217.3:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.153G>A
  hgvsp: ENST00000328268.4:c.153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.190G>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22781
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4397
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys51Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-50312904-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312904
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312904
    reference: chr 22
allele count: 1
allele frequency: 8.300270588821196e-6
allele num: 120478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.193C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.156C>T
  hgvsp: ENST00000404488.3:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.156C>T
  hgvsp: ENST00000328268.4:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.156C>T
  hgvsp: ENST00000407217.3:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.156C>T
  hgvsp: ENST00000450207.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.156C>T
  hgvsp: ENST00000403427.3:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.156C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9004
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn52Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

22-50312906-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312906
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312906
    reference: chr 22
allele count: 1
allele frequency: 8.302062232258493e-6
allele num: 120452
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.195T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.158T>C
  hgvsp: ENSP00000384111.3:p.Phe53Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.158T>C
  hgvsp: ENSP00000383938.3:p.Phe53Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.158T>C
  hgvsp: ENSP00000332223.4:p.Phe53Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.158T>C
  hgvsp: ENSP00000387769.1:p.Phe53Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.158T>C
  hgvsp: ENSP00000386034.3:p.Phe53Ser
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.158T>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7032
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4396
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Phe53Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

22-50312910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312910
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312910
    reference: chr 22
allele count: 1
allele frequency: 8.303854649328218e-6
allele num: 120426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.162C>T
  hgvsp: ENST00000403427.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.162C>T
  hgvsp: ENST00000328268.4:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.199C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.162C>T
  hgvsp: ENST00000450207.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.162C>T
  hgvsp: ENST00000404488.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.162C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.162C>T
  hgvsp: ENST00000407217.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18253
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14382
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3442
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2459
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly54Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

22-50312913-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312913
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312913
    reference: chr 22
allele count: 3
allele frequency: 2.490825459557297e-5
allele num: 120442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.165C>T
  hgvsp: ENST00000328268.4:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.165C>T
  hgvsp: ENST00000404488.3:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.165C>T
  hgvsp: ENST00000450207.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.202C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.165C>T
  hgvsp: ENST00000407217.3:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.165C>T
  hgvsp: ENST00000403427.3:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.165C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7029
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12837
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8994
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly55Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

22-50312914-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312914
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312914
    reference: chr 22
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.166G>T
  hgvsp: ENSP00000383938.3:p.Gly56Trp
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.203G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.166G>T
  hgvsp: ENSP00000332223.4:p.Gly56Trp
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.166G>T
  hgvsp: ENSP00000386034.3:p.Gly56Trp
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.166G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.166G>T
  hgvsp: ENSP00000387769.1:p.Gly56Trp
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.166G>T
  hgvsp: ENSP00000384111.3:p.Gly56Trp
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7026
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12835
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly56Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

22-50312915-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312915
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312915
    reference: chr 22
allele count: 2
allele frequency: 1.660495159656609e-5
allele num: 120446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.167G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.167G>A
  hgvsp: ENSP00000387769.1:p.Gly56Glu
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.167G>A
  hgvsp: ENSP00000332223.4:p.Gly56Glu
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.167G>A
  hgvsp: ENSP00000384111.3:p.Gly56Glu
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.204G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.167G>A
  hgvsp: ENSP00000386034.3:p.Gly56Glu
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.167G>A
  hgvsp: ENSP00000383938.3:p.Gly56Glu
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18278
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4394
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3218
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly56Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

22-50312916-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312916
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312916
    reference: chr 22
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.168G>C
  hgvsp: ENST00000404488.3:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.168G>C
  hgvsp: ENST00000403427.3:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.168G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.168G>C
  hgvsp: ENST00000407217.3:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.168G>C
  hgvsp: ENST00000450207.1:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.205G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.168G>C
  hgvsp: ENST00000328268.4:c.168G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18274
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12837
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly56Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

22-50312920-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312920
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312920
    reference: chr 22
allele count: 4
allele frequency: 3.321762527196931e-5
allele num: 120418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.172A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.209A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.172A>G
  hgvsp: ENSP00000384111.3:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.172A>G
  hgvsp: ENSP00000383938.3:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.172A>G
  hgvsp: ENSP00000332223.4:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.172A>G
  hgvsp: ENSP00000387769.1:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.172A>G
  hgvsp: ENSP00000386034.3:p.Thr58Ala
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1672
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3441
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr58Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/22-50312921-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312921
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312921
    reference: chr 22
allele count: 2
allele frequency: 1.66096402351925e-5
allele num: 120412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.173C>A
  hgvsp: ENSP00000332223.4:p.Thr58Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.210C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.173C>A
  hgvsp: ENSP00000384111.3:p.Thr58Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.173C>A
  hgvsp: ENSP00000383938.3:p.Thr58Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.173C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.173C>A
  hgvsp: ENSP00000387769.1:p.Thr58Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.173C>A
  hgvsp: ENSP00000386034.3:p.Thr58Lys
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18280
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr58Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

22-50312926-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312926
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312926
    reference: chr 22
allele count: 1
allele frequency: 8.306061763875276e-6
allele num: 120394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.215T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.178T>C
  hgvsp: ENSP00000387769.1:p.Trp60Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.178T>C
  hgvsp: ENSP00000386034.3:p.Trp60Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.178T>C
  hgvsp: ENSP00000384111.3:p.Trp60Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.178T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.178T>C
  hgvsp: ENSP00000332223.4:p.Trp60Arg
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.178T>C
  hgvsp: ENSP00000383938.3:p.Trp60Arg
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7031
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4389
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2458
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9001
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Trp60Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

22-50312934-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312934
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312934
    reference: chr 22
allele count: 27
allele frequency: 2.24397865726966e-4
allele num: 120322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.186A>G
  hgvsp: ENST00000328268.4:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.186A>G
  hgvsp: ENST00000450207.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.223A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.186A>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.186A>G
  hgvsp: ENST00000403427.3:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.186A>G
  hgvsp: ENST00000407217.3:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.186A>G
  hgvsp: ENST00000404488.3:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14341
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3431
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu62Glu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-50312939-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312939
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312939
    reference: chr 22
allele count: 1
allele frequency: 8.31282835672009e-6
allele num: 120296
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.191C>A
  hgvsp: ENSP00000383938.3:p.Thr64Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.191C>A
  hgvsp: ENSP00000384111.3:p.Thr64Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.228C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.191C>A
  hgvsp: ENSP00000386034.3:p.Thr64Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.191C>A
  hgvsp: ENSP00000387769.1:p.Thr64Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.191C>A
  hgvsp: ENSP00000332223.4:p.Thr64Lys
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.191C>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4387
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr64Lys
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/22-50312948-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312948
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312948
    reference: chr 22
allele count: 1
allele frequency: 8.317391665973551e-6
allele num: 120230
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.200A>C
  hgvsp: ENSP00000383938.3:p.Lys67Thr
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.200A>C
  hgvsp: ENSP00000387769.1:p.Lys67Thr
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.200A>C
  hgvsp: ENSP00000332223.4:p.Lys67Thr
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.200A>C
  hgvsp: ENSP00000384111.3:p.Lys67Thr
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.237A>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.200A>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.200A>C
  hgvsp: ENSP00000386034.3:p.Lys67Thr
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8972
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys67Thr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

22-50312952-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312952
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312952
    reference: chr 22
allele count: 1
allele frequency: 8.320990530712775e-6
allele num: 120178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.204C>T
  hgvsp: ENST00000328268.4:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.204C>T
  hgvsp: ENST00000407217.3:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.204C>T
  hgvsp: ENST00000403427.3:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.204C>T
  hgvsp: ENST00000450207.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.204C>T
  hgvsp: ENST00000404488.3:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.241C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.204C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3181
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12809
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3189
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8956
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr68Tyr
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

22-50312957-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312957
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312957
    reference: chr 22
allele count: 1
allele frequency: 8.325562808045825e-6
allele num: 120112
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.209C>T
  hgvsp: ENSP00000383938.3:p.Ser70Phe
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.209C>T
  hgvsp: ENSP00000384111.3:p.Ser70Phe
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.209C>T
  hgvsp: ENSP00000386034.3:p.Ser70Phe
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.209C>T
  hgvsp: ENSP00000387769.1:p.Ser70Phe
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.209C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.209C>T
  hgvsp: ENSP00000332223.4:p.Ser70Phe
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.246C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3182
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22209
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser70Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-50312966-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312966
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312966
    reference: chr 22
allele count: 1
allele frequency: 8.335695113615524e-6
allele num: 119966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+6T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+6T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+6T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+6T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+6T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+6T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+6T>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17694
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21744
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12796
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
hgvs: c.212+6T>C
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

22-50312971-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312971
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312971
    reference: chr 22
allele count: 1
allele frequency: 8.339588024351597e-6
allele num: 119910
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+11T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+11T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+11T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+11T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+11T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+11T>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+11T>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17459
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4262
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2435
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8561
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

22-50312973-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312973
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312973
    reference: chr 22
allele count: 1
allele frequency: 8.344877079960612e-6
allele num: 119834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+13G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+13G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+13G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+13G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+13G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+13G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+13G>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12781
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8459
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

22-50312976-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312976
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312976
    reference: chr 22
allele count: 34
allele frequency: 2.838821721995859e-4
allele num: 119768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+16C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+16C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17035
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6831
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20350
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4208
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8378
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3017
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12785
  bin: 9.75e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 3347
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

22-50312979-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312979
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312979
    reference: chr 22
allele count: 24875
allele frequency: 2.08110233585436e-1
allele num: 119528
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+19C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+19C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+19C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+19C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+19C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+19C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+19C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 1.75e1
  variant carriers: 647
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 7.5e0
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 5.75e1
  variant carriers: 1290
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.25e1
  variant carriers: 797
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 9.75e1
  variant carriers: 466
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3278
  bin: 4.75e1
  variant carriers: 2374
genotype depth: GenotypeDepth
  all individuals: 13186
  bin: 3.25e1
  variant carriers: 3076
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 1.25e1
  variant carriers: 263
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.75e1
  variant carriers: 240
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 4.25e1
  variant carriers: 2854
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 6.75e1
  variant carriers: 523
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 16463
  bin: 2.75e1
  variant carriers: 2319
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.25e1
  variant carriers: 373
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 8.25e1
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 2.25e1
  variant carriers: 1440
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 1688
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 3.75e1
  variant carriers: 3287
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 75
genotype quality: GenotypeQuality
  all individuals: 23727
  bin: 9.75e1
  variant carriers: 20550
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 8.75e1
  variant carriers: 101
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 2.25e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 5.25e1
  variant carriers: 82
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 3.25e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 3.75e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 5.75e1
  variant carriers: 72
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 8
num of homozygotes: 2963
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

22-50312981-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312981
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312981
    reference: chr 22
allele count: 1
allele frequency: 8.39545973537511e-6
allele num: 119112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+21C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+21C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+21C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+21C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+21C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+21C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+21C>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29865
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4289
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

22-50312989-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312989
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312989
    reference: chr 22
allele count: 1
allele frequency: 8.430139434506248e-6
allele num: 118622
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+29C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+29C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+29C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+29C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+29C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+29C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+29C>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13957
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4822
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4280
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2606
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2093
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1666
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

22-50312996-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50312996
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50312996
    reference: chr 22
allele count: 1
allele frequency: 8.456802652053312e-6
allele num: 118248
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+36T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+36T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+36T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+36T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+36T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+36T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+36T>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8616
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11802
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2983
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3847
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4274
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2055
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

22-50313000-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313000
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313000
    reference: chr 22
allele count: 1
allele frequency: 8.512521919743944e-6
allele num: 117474
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+40G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+40G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+40G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+40G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+40G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+40G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+40G>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11826
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1993
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5612
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16137
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

22-50313005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313005
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313005
    reference: chr 22
allele count: 1
allele frequency: 8.64707815229234e-6
allele num: 115646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+45C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+45C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+45C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+45C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+45C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+45C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+45C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10813
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11887
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4806
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5958
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5004
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3044
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2550
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2780
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

http://identifiers.org/exac.variant/22-50313006-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313006
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313006
    reference: chr 22
allele count: 1
allele frequency: 8.657558914688415e-6
allele num: 115506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+46C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+46C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+46C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+46C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+46C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+46C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+46C>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6345
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4605
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2838
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5384
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11200
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

22-50313006-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313006
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313006
    reference: chr 22
allele count: 1
allele frequency: 8.657558914688415e-6
allele num: 115506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+46C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+46C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+46C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+46C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+46C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+46C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+46C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12250
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2539
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4605
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5384
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4831
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2838
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

22-50313008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313008
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313008
    reference: chr 22
allele count: 1
allele frequency: 8.695954641900589e-6
allele num: 114996
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+48G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+48G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+48G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+48G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+48G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+48G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+48G>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11732
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4793
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6007
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8976
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

22-50313009-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313009
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313009
    reference: chr 22
allele count: 1
allele frequency: 8.684173961372795e-6
allele num: 115152
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.212+49G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.212+49G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.212+49G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.249+49G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.212+49G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.212+49G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.212+49G>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13031
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1890
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5378
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3150
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum

22-50313328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313328
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313328
    reference: chr 22
allele count: 1
allele frequency: 1.825817053131276e-5
allele num: 54770
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-50T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-50T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-50T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-50T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-50T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-50T>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-50T>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7608
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14778
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25010
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1790
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15418
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5303
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4024
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3707
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1635
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

22-50313331-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313331
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313331
    reference: chr 22
allele count: 3
allele frequency: 5.480853551593101e-5
allele num: 54736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-47C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-47C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-47C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-47C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-47C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-47C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-47C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7494
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14820
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5699
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1256
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17703
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4960
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

22-50313341-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313341
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313341
    reference: chr 22
allele count: 1
allele frequency: 1.76934781839414e-5
allele num: 56518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-37G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-37G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-37G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-37G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-37G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-37G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-37G>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25738
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4952
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2488
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22073
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3397
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5023
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2997
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

22-50313343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313343
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313343
    reference: chr 22
allele count: 1
allele frequency: 1.763730643056193e-5
allele num: 56698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-35C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-35C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-35C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-35C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-35C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-35C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-35C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14696
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22687
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4883
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

22-50313344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313344
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313344
    reference: chr 22
allele count: 1
allele frequency: 1.73816310922617e-5
allele num: 57532
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-34G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-34G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-34G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-34G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-34G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-34G>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-34G>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14346
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6022
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4990
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4517
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5979
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

22-50313344-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313344
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313344
    reference: chr 22
allele count: 9
allele frequency: 1.564346798303553e-4
allele num: 57532
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-34G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-34G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-34G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-34G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-34G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-34G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-34G>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14346
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4934
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26010
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2772
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23877
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1839
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1879
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4517
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5979
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS

22-50313345-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313345
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313345
    reference: chr 22
allele count: 3
allele frequency: 5.152691422486345e-5
allele num: 58222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-33C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-33C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-33C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-33C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-33C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-33C>G
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-33C>G
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26118
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2807
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6525
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4309
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1814
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/22-50313349-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313349
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313349
    reference: chr 22
allele count: 1
allele frequency: 1.69785052124011e-5
allele num: 58898
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-29C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-29C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-29C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-29C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-29C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-29C>A
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-29C>A
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26262
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13420
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6928
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3773
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24208
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4803
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

22-50313349-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313349
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313349
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 58898
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-29C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-29C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-29C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-29C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-29C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-29C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-29C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26262
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2509
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2683
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5588
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3773
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1810
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24208
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

22-50313350-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313350
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313350
    reference: chr 22
allele count: 1
allele frequency: 1.669616322169166e-5
allele num: 59894
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-28G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-28G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-28G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-28G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-28G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-28G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-28G>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13371
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4784
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2655
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5533
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3631
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

22-50313355-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313355
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313355
    reference: chr 22
allele count: 1
allele frequency: 1.588612823282709e-5
allele num: 62948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-23G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-23G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-23G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-23G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-23G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-23G>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-23G>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12981
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25415
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24538
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9147
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5272
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 760
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD

22-50313356-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313356
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313356
    reference: chr 22
allele count: 1
allele frequency: 1.578681485223541e-5
allele num: 63344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-22C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-22C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-22C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-22C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-22C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-22C>T
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-22C>T
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2965
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1586
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1825
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5130
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

22-50313358-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50313358
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 50313358
    reference: chr 22
allele count: 24216
allele frequency: 3.065549282223967e-1
allele num: 78994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000482956
  gene symbol: CRELD2
  hgvsc: ENST00000482956.1:n.213-20G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl transcript: ENST00000483652
  gene symbol: CRELD2
  hgvsc: ENST00000483652.1:n.250-20G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000387769
  ensembl transcript: ENST00000450207
  gene symbol: CRELD2
  hgvsc: ENST00000450207.1:c.213-20G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000383938
  ensembl transcript: ENST00000404488
  gene symbol: CRELD2
  hgvsc: ENST00000404488.3:c.213-20G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000332223
  ensembl transcript: ENST00000328268
  gene symbol: CRELD2
  hgvsc: ENST00000328268.4:c.213-20G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000386034
  ensembl transcript: ENST00000407217
  gene symbol: CRELD2
  hgvsc: ENST00000407217.3:c.213-20G>C
  variant of: http://identifiers.org/hgnc/28150
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000184164
  ensembl protein: ENSP00000384111
  ensembl transcript: ENST00000403427
  gene symbol: CRELD2
  hgvsc: ENST00000403427.3:c.213-20G>C
  variant of: http://identifiers.org/hgnc/28150
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 5.25e1
  variant carriers: 415
genotype depth: GenotypeDepth
  all individuals: 9583
  bin: 2.25e1
  variant carriers: 2806
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 2.75e1
  variant carriers: 1515
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.25e1
  variant carriers: 1001
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 6.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 3.75e1
  variant carriers: 903
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 57
genotype depth: GenotypeDepth
  all individuals: 17675
  bin: 7.5e0
  variant carriers: 2834
genotype depth: GenotypeDepth
  all individuals: 7178
  bin: 1.75e1
  variant carriers: 5288
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 2.5e0
  variant carriers: 145
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.25e1
  variant carriers: 777
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 265
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.25e1
  variant carriers: 197
genotype depth: GenotypeDepth
  all individuals: 13682
  bin: 1.25e1
  variant carriers: 6305
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.75e1
  variant carriers: 588
num of homozygotes: 3648
reference allele: G

GenotypeQuality
all individuals: 767
bin: 2.25e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3
bin: 6.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 7.142857142857142e-2
allele num: 28
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

FS
type: SiteQuality
SIO_000300: 4.371e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.9012e4

QD
type: SiteQuality
SIO_000300: 1.437e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.710000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 867
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 166
bin: 1.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.5e-1
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.58e-1

FS
type: SiteQuality
SIO_000300: 6.879999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 1.385e1

DP
type: SiteQuality
SIO_000300: 5.0426e4

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.859999999999999e-2

GenotypeQuality
all individuals: 14
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 2.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 19570
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 1.75e1
variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.458e0

QD
type: SiteQuality
SIO_000300: 8.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.002e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

DP
type: SiteQuality
SIO_000300: 6.298e4

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

GenotypeQuality
all individuals: 33
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 172
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 119
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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Latino
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African
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South Asian
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East Asian
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European (Finnish)
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BaseQRankSum
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DP
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QD
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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East Asian
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QD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Latino
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East Asian
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Other
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South Asian
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European (Finnish)
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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ClippingRankSum
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MQRankSum
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FS
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DP
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Other
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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African
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Other
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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Other
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European (Non-Finnish)
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Latino
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East Asian
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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BaseQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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FS
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QD
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MQ
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ClippingRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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VQSLOD
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QD
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MQRankSum
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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Latino
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African
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East Asian
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South Asian
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QD
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ReadPosRankSum
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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MQ
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QD
type: SiteQuality
SIO_000300: 1.094e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65414
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.263e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

FS
type: SiteQuality
SIO_000300: 9.151e0

QD
type: SiteQuality
SIO_000300: 9.15e0

MQRankSum
type: SiteQuality
SIO_000300: 4.24e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

DP
type: SiteQuality
SIO_000300: 2.214541e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 492
bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528724737823707e-5
allele num: 65414
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.15e0

VQSLOD
type: SiteQuality
SIO_000300: -3.263e0

MQRankSum
type: SiteQuality
SIO_000300: 4.24e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

FS
type: SiteQuality
SIO_000300: 9.151e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

DP
type: SiteQuality
SIO_000300: 2.214541e6

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

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

African
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allele count: 5
allele frequency: 4.91448791035974e-4
allele num: 10174
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65400
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.446e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

QD
type: SiteQuality
SIO_000300: 1.202e1

MQ
type: SiteQuality
SIO_000300: 5.333e1

DP
type: SiteQuality
SIO_000300: 2.215269e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.609e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 10

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.526018617427133e-4
allele num: 65530
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.582e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.122e0

MQ
type: SiteQuality
SIO_000300: 5.479e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 4.124e0

DP
type: SiteQuality
SIO_000300: 2.225159e6

QD
type: SiteQuality
SIO_000300: 1.049e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.515151515151515e-4
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65530
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.124e0

MQ
type: SiteQuality
SIO_000300: 5.479e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

VQSLOD
type: SiteQuality
SIO_000300: -1.122e0

QD
type: SiteQuality
SIO_000300: 1.049e1

DP
type: SiteQuality
SIO_000300: 2.225159e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.02e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.582e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65556
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 6.807e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.496e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.841e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.476e0

QD
type: SiteQuality
SIO_000300: 8.99e0

DP
type: SiteQuality
SIO_000300: 2.227684e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 80

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.792207792207792e-4
allele num: 11550
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.252252252252252e-3
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.750390015600624e-5
allele num: 10256
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.252217227554368e-4
allele num: 16462
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 61
allele frequency: 9.291698400609292e-4
allele num: 65650
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e0

MQRankSum
type: SiteQuality
SIO_000300: -1.356e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-2

MQ
type: SiteQuality
SIO_000300: 5.576e1

FS
type: SiteQuality
SIO_000300: 1.251e0

DP
type: SiteQuality
SIO_000300: 2.234031e6

QD
type: SiteQuality
SIO_000300: 1.219e1

VQSLOD
type: SiteQuality
SIO_000300: -1.451e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.56e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65688
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 1.821272462360369e-4
allele num: 16472
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.084e0

FS
type: SiteQuality
SIO_000300: 1.0219e1

DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.2e-3

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 103
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GenotypeQuality
all individuals: 2949
bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.522162688748173e-5
allele num: 65696
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.42e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
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VQSLOD
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521005080156968e-5
allele num: 65746
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.412e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

VQSLOD
type: SiteQuality
SIO_000300: 8.34e-1

DP
type: SiteQuality
SIO_000300: 2.235422e6

QD
type: SiteQuality
SIO_000300: 1.276e1

FS
type: SiteQuality
SIO_000300: 1.609e0

MQRankSum
type: SiteQuality
SIO_000300: 9.320000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 19860
bin: 9.75e1
variant carriers: 12960

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 20623
bin: 6.25e1
variant carriers: 7

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7884
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2668
bin: 7.25e1
variant carriers: 8

East Asian
type: Population
allele count: 282
allele frequency: 3.274500696702276e-2
allele num: 8612
num of homozygotes: 4

European (Non-Finnish)
type: Population
allele count: 7889
allele frequency: 1.198062203863443e-1
allele num: 65848
num of homozygotes: 464

Other
type: Population
allele count: 70
allele frequency: 7.865168539325842e-2
allele num: 890
num of homozygotes: 6

South Asian
type: Population
allele count: 2632
allele frequency: 1.595151515151515e-1
allele num: 16500
num of homozygotes: 237

European (Finnish)
type: Population
allele count: 757
allele frequency: 1.145927944293067e-1
allele num: 6606
num of homozygotes: 47

Latino
type: Population
allele count: 778
allele frequency: 6.73359875367838e-2
allele num: 11554
num of homozygotes: 29

African
type: Population
allele count: 1559
allele frequency: 1.511537715726197e-1
allele num: 10314
num of homozygotes: 124

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.95e-1

MQ
type: SiteQuality
SIO_000300: 5.627e1

FS
type: SiteQuality
SIO_000300: 1.173e0

MQRankSum
type: SiteQuality
SIO_000300: -1.328e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

DP
type: SiteQuality
SIO_000300: 2.686086e6

QD
type: SiteQuality
SIO_000300: 1.318e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.82e-1

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3445
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22612
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65850
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -5.938e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 5.39e-1

MQ
type: SiteQuality
SIO_000300: 5.621e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.742e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

DP
type: SiteQuality
SIO_000300: 2.117877e6

QD
type: SiteQuality
SIO_000300: 1.811e1

GenotypeQuality
all individuals: 22722
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1671
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2462
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517773123273533e-5
allele num: 65886
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: -5.094e-1

QD
type: SiteQuality
SIO_000300: 1.059e1

MQRankSum
type: SiteQuality
SIO_000300: -1.441e0

FS
type: SiteQuality
SIO_000300: 4.457e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.202e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 2.119099e6

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3442
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22761
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9004
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4392
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12856
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1672
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65914
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.368e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.717e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.171e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.119391e6

MQ
type: SiteQuality
SIO_000300: 5.787e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.48e-1

GenotypeQuality
all individuals: 9006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 12852
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1673
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22780
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2462
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.032508491023775e-5
allele num: 65952
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.120098e6

VQSLOD
type: SiteQuality
SIO_000300: 4.22e-1

QD
type: SiteQuality
SIO_000300: 1.027e1

FS
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

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

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

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22838
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12846
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.759e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.491e0

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-1

DP
type: SiteQuality
SIO_000300: 2.120422e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.198e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.73e1

GenotypeQuality
all individuals: 3446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12845
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9009
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1673
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65982
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.709e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 1.646e0

VQSLOD
type: SiteQuality
SIO_000300: -1.652e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

DP
type: SiteQuality
SIO_000300: 2.120211e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e-1

QD
type: SiteQuality
SIO_000300: 1.235e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.927e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

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

GenotypeQuality
all individuals: 34
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3222
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3447
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12843
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65978
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.185e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

FS
type: SiteQuality
SIO_000300: 1.293e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

DP
type: SiteQuality
SIO_000300: 2.12022e6

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22672
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9005
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12842
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3446
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1674
bin: 8.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516024377671993e-5
allele num: 65962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.41e-1

QD
type: SiteQuality
SIO_000300: 1.536e1

DP
type: SiteQuality
SIO_000300: 2.119758e6

FS
type: SiteQuality
SIO_000300: 6.860000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.98e0

VQSLOD
type: SiteQuality
SIO_000300: -1.181e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.409e0

MQRankSum
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 5.668e1

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8994
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 65940
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 1.51285930408472e-4
allele num: 6610
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.516162290011523e-5
allele num: 65956
num of homozygotes: 0

South Asian
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allele frequency: 6.05766900896535e-5
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QD
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InbreedingCoeff
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FS
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VQSLOD
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ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.515932450050026e-5
allele num: 65966
num of homozygotes: 0

African
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allele frequency: 0.0e0
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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QD
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BaseQRankSum
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InbreedingCoeff
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DP
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SIO_000300: 2.119354e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

Latino
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South Asian
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East Asian
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allele frequency: 1.160092807424594e-4
allele num: 8620
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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FS
type: SiteQuality
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DP
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ClippingRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.033520400424693e-5
allele num: 65930
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European (Finnish)
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allele frequency: 3.026634382566586e-4
allele num: 6608
num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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FS
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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European (Finnish)
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African
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East Asian
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South Asian
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Latino
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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QD
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BaseQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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African
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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allele num: 65828
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

FS
type: SiteQuality
SIO_000300: 9.317e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.47e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.31e1

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.14e0

DP
type: SiteQuality
SIO_000300: 2.115456e6

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
all individuals: 1671
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22480
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3428
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65778
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.745e-1

QD
type: SiteQuality
SIO_000300: 1.131e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.698e1

DP
type: SiteQuality
SIO_000300: 2.11267e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.92e-1

GenotypeQuality
all individuals: 149
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3423
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variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65752
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.110983e6

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.083e0

MQ
type: SiteQuality
SIO_000300: 5.646e1

QD
type: SiteQuality
SIO_000300: 9.66e0

GenotypeQuality
all individuals: 201
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8890
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variant carriers: 0

GenotypeQuality
all individuals: 3175
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.748488984207447e-5
allele num: 10258
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 1.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.91e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 2.107865e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.831e0

QD
type: SiteQuality
SIO_000300: 1.212e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.194e0

GenotypeQuality
all individuals: 3111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 72
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GenotypeQuality
all individuals: 2446
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524157902758726e-5
allele num: 65610
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.317e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

MQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.821e0

QD
type: SiteQuality
SIO_000300: 1.466e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.24e-1

FS
type: SiteQuality
SIO_000300: 2.136e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.69e-1

DP
type: SiteQuality
SIO_000300: 2.097729e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
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variant carriers: 0

GenotypeQuality
all individuals: 366
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variant carriers: 0

GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 3370
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variant carriers: 0

GenotypeQuality
all individuals: 1646
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variant carriers: 0

GenotypeQuality
all individuals: 12786
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variant carriers: 1

GenotypeQuality
all individuals: 3059
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variant carriers: 0

GenotypeQuality
all individuals: 21453
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65598
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.387e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

DP
type: SiteQuality
SIO_000300: 2.090622e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

FS
type: SiteQuality
SIO_000300: 4.286e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.24e0

GenotypeQuality
all individuals: 1641
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 444
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GenotypeQuality
all individuals: 4241
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 252
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variant carriers: 0

GenotypeQuality
all individuals: 20692
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2431
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525599560627327e-5
allele num: 65548
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e0

QD
type: SiteQuality
SIO_000300: 2.452e1

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.093e0

VQSLOD
type: SiteQuality
SIO_000300: -2.393e0

DP
type: SiteQuality
SIO_000300: 2.083368e6

GenotypeQuality
all individuals: 400
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 562
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GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 1044
bin: 2.25e1
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GenotypeQuality
all individuals: 1634
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
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variant carriers: 0

GenotypeQuality
all individuals: 2430
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65494
num of homozygotes: 0

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

African
type: Population
allele count: 31
allele frequency: 3.030895580758702e-3
allele num: 10228
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.605976372480889e-4
allele num: 11512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

DP
type: SiteQuality
SIO_000300: 2.078467e6

QD
type: SiteQuality
SIO_000300: 1.31e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.251e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

GenotypeQuality
all individuals: 73
bin: 1.75e1
variant carriers: 26

GenotypeQuality
all individuals: 1903
bin: 8.25e1
variant carriers: 170

GenotypeQuality
all individuals: 1187
bin: 9.25e1
variant carriers: 183

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 48

GenotypeQuality
all individuals: 17672
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variant carriers: 119

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 6722
bin: 6.75e1
variant carriers: 148

GenotypeQuality
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variant carriers: 19

GenotypeQuality
all individuals: 2749
bin: 7.75e1
variant carriers: 189

GenotypeQuality
all individuals: 2140
bin: 7.25e1
variant carriers: 119

Other
type: Population
allele count: 154
allele frequency: 1.738148984198646e-1
allele num: 886
num of homozygotes: 19

European (Non-Finnish)
type: Population
allele count: 12526
allele frequency: 1.916521313381682e-1
allele num: 65358
num of homozygotes: 1155

European (Finnish)
type: Population
allele count: 977
allele frequency: 1.494798041615667e-1
allele num: 6536
num of homozygotes: 68

Latino
type: Population
allele count: 1239
allele frequency: 1.078704509838064e-1
allele num: 11486
num of homozygotes: 79

South Asian
type: Population
allele count: 5731
allele frequency: 3.479237493929092e-1
allele num: 16472
num of homozygotes: 1017

East Asian
type: Population
allele count: 710
allele frequency: 8.286647992530345e-2
allele num: 8568
num of homozygotes: 27

African
type: Population
allele count: 3538
allele frequency: 3.461162199178243e-1
allele num: 10222
num of homozygotes: 598

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.62e-2

DP
type: SiteQuality
SIO_000300: 2.113033e6

MQRankSum
type: SiteQuality
SIO_000300: -5.03e-1

QD
type: SiteQuality
SIO_000300: 1.483e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

MQ
type: SiteQuality
SIO_000300: 5.753e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.206e0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2860
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GenotypeQuality
all individuals: 166
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GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 10101
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GenotypeQuality
all individuals: 1208
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GenotypeQuality
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GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 3429
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.537515375153752e-4
allele num: 6504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65148
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.669e0

QD
type: SiteQuality
SIO_000300: 1.798e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.224e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-1

MQ
type: SiteQuality
SIO_000300: 5.5e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

DP
type: SiteQuality
SIO_000300: 1.817867e6

GenotypeQuality
all individuals: 4688
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2638
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64858
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.904912836767037e-5
allele num: 10096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16338
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.787e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.002e0

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.6e-1

DP
type: SiteQuality
SIO_000300: 1.720468e6

VQSLOD
type: SiteQuality
SIO_000300: -2.155e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.3e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.137981831573779e-5
allele num: 16292
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10030
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64656
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.274e0

MQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.051e0

QD
type: SiteQuality
SIO_000300: 1.037e1

VQSLOD
type: SiteQuality
SIO_000300: 5.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.653338e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64226
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.184553423359394e-4
allele num: 8442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9940
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.208e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.927e0

MQRankSum
type: SiteQuality
SIO_000300: 2.45e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.265e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

DP
type: SiteQuality
SIO_000300: 1.596941e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.26e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11228
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.580278128950695e-5
allele num: 63280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6288
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.609e0

FS
type: SiteQuality
SIO_000300: 2.049e0

QD
type: SiteQuality
SIO_000300: 1.28e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.547184e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.9e-1

GenotypeQuality
all individuals: 505
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4831
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.292474200855777e-5
allele num: 15892
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.809e0

DP
type: SiteQuality
SIO_000300: 1.54618e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.061e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

MQ
type: SiteQuality
SIO_000300: 5.787e1

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

QD
type: SiteQuality
SIO_000300: 1.123e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1888
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GenotypeQuality
all individuals: 11200
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.581627811343435e-5
allele num: 63226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8352
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

DP
type: SiteQuality
SIO_000300: 1.54618e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.061e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.809e0

MQ
type: SiteQuality
SIO_000300: 5.787e1

QD
type: SiteQuality
SIO_000300: 1.123e1

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 1.037129226301597e-4
allele num: 9642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15838
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62924
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.976e0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.711e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62992
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6280
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African
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allele frequency: 0.0e0
allele num: 9700
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.205400192864031e-4
allele num: 8296
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.535644e6

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.43e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.265839320705422e-5
allele num: 30620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2008
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9962
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3184
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.55e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 7.14209e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1790
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
all individuals: 119
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GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3754
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
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South Asian
type: Population
allele count: 3
allele frequency: 3.013258336681398e-4
allele num: 9956
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1998
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MQRankSum
type: SiteQuality
SIO_000300: -5.23e-1

DP
type: SiteQuality
SIO_000300: 7.21957e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.725e0

MQ
type: SiteQuality
SIO_000300: 5.919e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.11e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4910
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2080
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 3.161955353190413e-5
allele num: 31626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3986
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3334
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.274e1

FS
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MQRankSum
type: SiteQuality
SIO_000300: -2.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

DP
type: SiteQuality
SIO_000300: 7.59753e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10130
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 4004
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2094
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3352
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4956
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.151392915668725e-5
allele num: 31732
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 430
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.855e1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.82e1

DP
type: SiteQuality
SIO_000300: 7.6811e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.513e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.36e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2136
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.110613412965037e-5
allele num: 32148
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4994
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 4134
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 7.83246e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

FS
type: SiteQuality
SIO_000300: 2.025e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4994
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3444
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 4.837929366231253e-4
allele num: 4134
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 2.177429389075526e-4
allele num: 32148
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2136
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.83246e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.337e1

FS
type: SiteQuality
SIO_000300: 2.025e0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2168
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 456
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4204
num of homozygotes: 0

African
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allele count: 3
allele frequency: 5.94059405940594e-4
allele num: 5050
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 32576
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.419e-1

DP
type: SiteQuality
SIO_000300: 7.88933e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1810
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5084
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.033980582524272e-5
allele num: 32960
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.24e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5084
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4296
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 32960
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 3576
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2186
num of homozygotes: 0

Other
type: Population
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allele num: 458
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
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MQRankSum
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 5176
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4444
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European (Finnish)
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allele count: 1
allele frequency: 4.472271914132379e-4
allele num: 2236
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 33502
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.387e1

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Other
type: Population
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allele frequency: 0.0e0
allele num: 478
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Latino
type: Population
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2382
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.835431552682318e-5
allele num: 35268
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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DP
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
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FS
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VQSLOD
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4780
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3990
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 35484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5476
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.074688796680498e-3
allele num: 482
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.60601e5

VQSLOD
type: SiteQuality
SIO_000300: -2.644e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.92e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.826e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-1

FS
type: SiteQuality
SIO_000300: 3.491e0

QD
type: SiteQuality
SIO_000300: 3.71e0