10-7621993-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7621993
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7621993
    reference: chr 10
allele count: 1
allele frequency: 9.988413440409126e-6
allele num: 100116
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1143C>G
  hgvsp: ENSP00000256861.6:p.Ile381Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1143C>G
  hgvsp: ENSP00000380332.2:p.Ile381Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.768C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1143C>G
  hgvsp: ENSP00000380333.2:p.Ile381Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*229C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.489C>G
  hgvsp: ENSP00000387969.2:p.Ile163Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.501C>G
  hgvsp: ENSP00000298441.6:p.Ile167Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5686C>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15646
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3317
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3724
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ile381Met
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-7621998-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7621998
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7621998
    reference: chr 10
allele count: 1
allele frequency: 1.031012867040581e-5
allele num: 96992
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.496G>C
  hgvsp: ENSP00000298441.6:p.Ala166Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*224G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.484G>C
  hgvsp: ENSP00000387969.2:p.Ala162Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5681G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1138G>C
  hgvsp: ENSP00000380332.2:p.Ala380Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1138G>C
  hgvsp: ENSP00000380333.2:p.Ala380Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.763G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1138G>C
  hgvsp: ENSP00000256861.6:p.Ala380Pro
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21719
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4265
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala380Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

10-7621998-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7621998
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7621998
    reference: chr 10
allele count: 1
allele frequency: 1.031012867040581e-5
allele num: 96992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1138G>A
  hgvsp: ENSP00000380333.2:p.Ala380Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1138G>A
  hgvsp: ENSP00000380332.2:p.Ala380Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.496G>A
  hgvsp: ENSP00000298441.6:p.Ala166Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.763G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*224G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1138G>A
  hgvsp: ENSP00000256861.6:p.Ala380Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5681G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.484G>A
  hgvsp: ENSP00000387969.2:p.Ala162Thr
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17717
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3788
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1051
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4265
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21719
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala380Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

10-7622002-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622002
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622003
    reference: chr 10
allele count: 2
allele frequency: 2.113003423065545e-5
allele num: 94652
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1133dupA
  hgvsp: ENSP00000380333.2:p.Arg379GlufsTer99
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1133dupA
  hgvsp: ENSP00000380332.2:p.Arg379GlufsTer99
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5676dupA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1133dupA
  hgvsp: ENSP00000256861.6:p.Arg379GlufsTer99
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.491dupA
  hgvsp: ENSP00000298441.6:p.Arg165GlufsTer99
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.758dupA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.479dupA
  hgvsp: ENSP00000387969.2:p.Arg161GlufsTer99
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*219dupA
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8408
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19334
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9456
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2278
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2810
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22948
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4212
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg379GlufsTer99
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

10-7622007-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622007
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622007
    reference: chr 10
allele count: 1
allele frequency: 1.090536325765011e-5
allele num: 91698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.475C>A
  hgvsp: ENSP00000387969.2:p.Leu159Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1129C>A
  hgvsp: ENSP00000380333.2:p.Leu377Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1129C>A
  hgvsp: ENSP00000256861.6:p.Leu377Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1129C>A
  hgvsp: ENSP00000380332.2:p.Leu377Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5672C>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*215C>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.487C>A
  hgvsp: ENSP00000298441.6:p.Leu163Met
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.754C>A
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 20595
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8772
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12703
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1209
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1334
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu377Met
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

10-7622008-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622008
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622008
    reference: chr 10
allele count: 1
allele frequency: 1.090631475624387e-5
allele num: 91690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1128C>G
  hgvsp: ENST00000397146.2:c.1128C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*214C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5671C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.753C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1128C>G
  hgvsp: ENST00000256861.6:c.1128C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.486C>G
  hgvsp: ENST00000298441.6:c.486C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.474C>G
  hgvsp: ENST00000446830.2:c.474C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1128C>G
  hgvsp: ENST00000397145.2:c.1128C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5004
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala376Ala
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

10-7622009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622009
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622009
    reference: chr 10
allele count: 9970
allele frequency: 1.103730764972877e-1
allele num: 90330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.485C>T
  hgvsp: ENSP00000298441.6:p.Ala162Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.473C>T
  hgvsp: ENSP00000387969.2:p.Ala158Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5670C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1127C>T
  hgvsp: ENSP00000256861.6:p.Ala376Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1127C>T
  hgvsp: ENSP00000380333.2:p.Ala376Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.752C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*213C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1127C>T
  hgvsp: ENSP00000380332.2:p.Ala376Val
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 259
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 8646
  bin: 2.25e1
  variant carriers: 1662
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 2.75e1
  variant carriers: 825
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 1.75e1
  variant carriers: 2805
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 2.5e0
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 20834
  bin: 1.25e1
  variant carriers: 2540
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 3.25e1
  variant carriers: 456
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 12931
  bin: 7.5e0
  variant carriers: 817
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.75e1
  variant carriers: 300
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 5.25e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 224
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 5.75e1
  variant carriers: 117
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 9.25e1
  variant carriers: 189
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 1.25e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 2.5e0
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1615
  bin: 3.75e1
  variant carriers: 87
genotype quality: GenotypeQuality
  all individuals: 10790
  bin: 6.25e1
  variant carriers: 121
genotype quality: GenotypeQuality
  all individuals: 3615
  bin: 3.25e1
  variant carriers: 78
hgvs: p.Ala376Val
num of homozygotes: 496
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum

10-7622010-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622010
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622010
    reference: chr 10
allele count: 22
allele frequency: 2.555702702074766e-4
allele num: 86082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*212G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.472G>C
  hgvsp: ENSP00000387969.2:p.Ala158Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5669G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1126G>C
  hgvsp: ENSP00000380333.2:p.Ala376Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.751G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1126G>C
  hgvsp: ENSP00000380332.2:p.Ala376Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1126G>C
  hgvsp: ENSP00000256861.6:p.Ala376Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.484G>C
  hgvsp: ENSP00000298441.6:p.Ala162Pro
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15132
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7741
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6700
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3848
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22408
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12522
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2319
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4397
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala376Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

10-7622014-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622014
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622014
    reference: chr 10
allele count: 2
allele frequency: 2.426831044022715e-5
allele num: 82412
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1122C>T
  hgvsp: ENST00000256861.6:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.480C>T
  hgvsp: ENST00000298441.6:c.480C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*208C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.468C>T
  hgvsp: ENST00000446830.2:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1122C>T
  hgvsp: ENST00000397145.2:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.747C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1122C>T
  hgvsp: ENST00000397146.2:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5665C>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6483
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27890
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4799
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1494
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3246
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2080
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn374Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

10-7622015-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622015
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622015
    reference: chr 10
allele count: 1
allele frequency: 1.205661787755299e-5
allele num: 82942
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*207A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.479A>G
  hgvsp: ENSP00000298441.6:p.Asn160Ser
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.467A>G
  hgvsp: ENSP00000387969.2:p.Asn156Ser
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1121A>G
  hgvsp: ENSP00000380333.2:p.Asn374Ser
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1121A>G
  hgvsp: ENSP00000380332.2:p.Asn374Ser
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5664A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.746A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1121A>G
  hgvsp: ENSP00000256861.6:p.Asn374Ser
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2886
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23155
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15985
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1144
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4844
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asn374Ser
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-7622019-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622019
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622019
    reference: chr 10
allele count: 1
allele frequency: 1.244771957777335e-5
allele num: 80336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*203A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.463A>G
  hgvsp: ENSP00000387969.2:p.Ile155Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1117A>G
  hgvsp: ENSP00000380332.2:p.Ile373Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1117A>G
  hgvsp: ENSP00000256861.6:p.Ile373Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.742A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5660A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1117A>G
  hgvsp: ENSP00000380333.2:p.Ile373Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.475A>G
  hgvsp: ENSP00000298441.6:p.Ile159Val
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5722
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16459
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4088
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile373Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

10-7622028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622028
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622028
    reference: chr 10
allele count: 1
allele frequency: 1.315962626661403e-5
allele num: 75990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-1G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-1G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-1G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-1G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-1G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-1G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-1G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-1G>A
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17526
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2563
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 639
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26350
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5180
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 1.25e1
  variant carriers: 0
hgvs: c.1109-1G>A
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/10-7622037-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622037
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622037
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 68694
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-10T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-10T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-10T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-10T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-10T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-10T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-10T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-10T>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 19846
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4967
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20072
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5625
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4011
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4365
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5031
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

10-7622044-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622044
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622044
    reference: chr 10
allele count: 1
allele frequency: 1.684749646202574e-5
allele num: 59356
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-17G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-17G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-17G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-17G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-17G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-17G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-17G>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-17G>C
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22312
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17780
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5463
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5206
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2174
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

10-7622044-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622044
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622044
    reference: chr 10
allele count: 2
allele frequency: 3.369499292405148e-5
allele num: 59356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-17G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-17G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-17G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-17G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-17G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-17G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-17G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-17G>A
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17780
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22312
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5206
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5463
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4614
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1877
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2174
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

10-7622045-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622045
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622045
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 63134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-18C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-18C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-18C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-18C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-18C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-18C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-18C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-18C>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18205
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21908
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5776
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16396
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7500
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2645
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.25e1
  variant carriers: 0
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: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

10-7622046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622046
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622046
    reference: chr 10
allele count: 2
allele frequency: 3.19744204636291e-5
allele num: 62550
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-19C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-19C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-19C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-19C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-19C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-19C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-19C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-19C>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18239
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4971
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8310
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4779
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/10-7622047-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622047
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622047
    reference: chr 10
allele count: 1
allele frequency: 1.521282745611099e-5
allele num: 65734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-20T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-20T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-20T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-20T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-20T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-20T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-20T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-20T>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21919
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5270
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1723
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8576
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

10-7622047-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622047
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622047
    reference: chr 10
allele count: 57951
allele frequency: 8.815985639090882e-1
allele num: 65734
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-20T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-20T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-20T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-20T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-20T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-20T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-20T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-20T>C
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.5e0
  variant carriers: 3157
genotype depth: GenotypeDepth
  all individuals: 21919
  bin: 7.5e0
  variant carriers: 20506
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 18119
  bin: 1.25e1
  variant carriers: 17579
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 310
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 594
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 2019
genotype depth: GenotypeDepth
  all individuals: 7390
  bin: 1.75e1
  variant carriers: 7304
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 2.25e1
  variant carriers: 3425
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 3.25e1
  variant carriers: 1147
genotype quality: GenotypeQuality
  all individuals: 6294
  bin: 1.75e1
  variant carriers: 6250
genotype quality: GenotypeQuality
  all individuals: 1723
  bin: 2.5e0
  variant carriers: 161
genotype quality: GenotypeQuality
  all individuals: 1332
  bin: 6.25e1
  variant carriers: 1220
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 1.25e1
  variant carriers: 2203
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 7.5e0
  variant carriers: 1325
genotype quality: GenotypeQuality
  all individuals: 2093
  bin: 5.25e1
  variant carriers: 2092
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 5.75e1
  variant carriers: 944
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 7.75e1
  variant carriers: 824
num of homozygotes: 25546
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

http://identifiers.org/exac.variant/10-7622054-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622054
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622054
    reference: chr 10
allele count: 7
allele frequency: 1.866368047779022e-4
allele num: 37506
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-27G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-27G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-27G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-27G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-27G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-27G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-27G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-27G>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14200
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13396
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24937
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19419
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1326
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4945
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2840
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/10-7622059-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622059
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622059
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 39562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-32G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-32G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-32G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-32G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-32G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-32G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-32G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-32G>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 25180
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14378
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2980
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16974
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4734
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22709
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

10-7622062-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622062
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622062
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 38238
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-35A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-35A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-35A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-35A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-35A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-35A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-35A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-35A>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14271
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25700
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5453
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1919
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

10-7622074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622074
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622074
    reference: chr 10
allele count: 19
allele frequency: 5.944931163954943e-4
allele num: 31960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-47G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-47G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-47G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-47G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-47G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-47G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-47G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-47G>A
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10872
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13099
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26908
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2784
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1753
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

10-7622075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622075
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622075
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 36732
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-48C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-48C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-48C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-48C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-48C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-48C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-48C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-48C>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27472
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9673
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2901
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4887
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3396
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10547
  bin: 1.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

10-7622075-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7622075
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7622075
    reference: chr 10
allele count: 31914
allele frequency: 8.688337144723947e-1
allele num: 36732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5652-48C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1109-48C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*195-48C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.467-48C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.455-48C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1109-48C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.734-48C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1109-48C>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 9673
  bin: 2.5e0
  variant carriers: 8439
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 2.25e1
  variant carriers: 1679
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.25e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 11299
  bin: 1.25e1
  variant carriers: 10961
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 2.75e1
  variant carriers: 671
genotype depth: GenotypeDepth
  all individuals: 27472
  bin: 7.5e0
  variant carriers: 25439
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.25e1
  variant carriers: 338
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 1.75e1
  variant carriers: 4027
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 5478
  bin: 9.75e1
  variant carriers: 5471
genotype quality: GenotypeQuality
  all individuals: 10547
  bin: 1.75e1
  variant carriers: 10425
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 4.25e1
  variant carriers: 1069
genotype quality: GenotypeQuality
  all individuals: 4887
  bin: 1.25e1
  variant carriers: 4748
genotype quality: GenotypeQuality
  all individuals: 4096
  bin: 7.5e0
  variant carriers: 3611
genotype quality: GenotypeQuality
  all individuals: 3396
  bin: 2.75e1
  variant carriers: 3341
genotype quality: GenotypeQuality
  all individuals: 2612
  bin: 2.5e0
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 2901
  bin: 3.75e1
  variant carriers: 2865
num of homozygotes: 13890
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

10-7627813-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627813
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627813
    reference: chr 10
allele count: 1
allele frequency: 8.987956138774043e-6
allele num: 111260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+51T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+51T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+51T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+51T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+51T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+51T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+51T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+51T>C
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2280
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5879
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2701
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2677
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3359
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-7627815-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627815
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627815
    reference: chr 10
allele count: 4
allele frequency: 3.448632617167293e-5
allele num: 115988
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+49T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+49T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+49T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+49T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+49T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+49T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+49T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+49T>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14194
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6324
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1833
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2611
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2781
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/10-7627816-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627816
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627816
    reference: chr 10
allele count: 6
allele frequency: 5.196154845414394e-5
allele num: 115470
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+48T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+48T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+48T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+48T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+48T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+48T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+48T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+48T>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14303
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9906
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9302
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2643
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2745
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-7627817-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627817
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627817
    reference: chr 10
allele count: 319
allele frequency: 4.509981338008257e-3
allele num: 70732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+47G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+47G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+47G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+47G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+47G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+47G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+47G>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+47G>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8440
  bin: 3.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 5.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 13918
  bin: 2.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11376
  bin: 2.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 4.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 1.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 7.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2921
  bin: 3.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 2525
  bin: 1.25e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 7.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 3132
  bin: 3.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 5.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 4.25e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 16900
  bin: 2.5e0
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 9902
  bin: 6.25e1
  variant carriers: 12
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/10-7627818-A-AAAAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627818
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627822
    reference: chr 10
allele count: 1
allele frequency: 8.73591333973967e-6
allele num: 114470
alternate allele: AAAAC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+45_*194+46insGTTT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+45_454+46insGTTT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+45_733+46insGTTT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+45_5651+46insGTTT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+45_1108+46insGTTT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+45_466+46insGTTT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+45_1108+46insGTTT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+45_1108+46insGTTT
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3235
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

10-7627818-ATTATTTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627818
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627811
    reference: chr 10
allele count: 1
allele frequency: 8.73591333973967e-6
allele num: 114470
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+39_1108+45delGAAATAA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+39_733+45delGAAATAA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+39_5651+45delGAAATAA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+39_454+45delGAAATAA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+39_466+45delGAAATAA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+39_*194+45delGAAATAA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+39_1108+45delGAAATAA
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+39_1108+45delGAAATAA
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19474
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8472
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: ATTATTTC
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-7627821-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627821
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627821
    reference: chr 10
allele count: 17
allele frequency: 1.507653558949254e-4
allele num: 112758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+43T>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+43T>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+43T>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+43T>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+43T>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+43T>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+43T>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+43T>A
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3524
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20831
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8918
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14090
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1621
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 3.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

10-7627822-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627822
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627822
    reference: chr 10
allele count: 2
allele frequency: 1.724762413977475e-5
allele num: 115958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+42A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+42A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+42A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+42A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+42A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+42A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+42A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+42A>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15147
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

10-7627830-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627830
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627830
    reference: chr 10
allele count: 1
allele frequency: 8.513246611727849e-6
allele num: 117464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+34G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+34G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+34G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+34G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+34G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+34G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+34G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+34G>A
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8735
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8551
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2328
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/10-7627832-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627832
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627832
    reference: chr 10
allele count: 1
allele frequency: 8.474719910506958e-6
allele num: 117998
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+32T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+32T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+32T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+32T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+32T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+32T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+32T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+32T>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8750
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1826
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/10-7627836-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627836
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627835
    reference: chr 10
allele count: 1
allele frequency: 8.442523301364311e-6
allele num: 118448
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+27delT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+27delT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+27delT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+27delT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+27delT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+27delT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+27delT
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+27delT
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8789
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 961
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8648
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2308
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: CA
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/10-7627838-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627838
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627838
    reference: chr 10
allele count: 1
allele frequency: 8.42034355001684e-6
allele num: 118760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+26T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+26T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+26T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+26T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+26T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+26T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+26T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+26T>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8690
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP

10-7627839-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627839
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627839
    reference: chr 10
allele count: 5
allele frequency: 4.207408404719029e-5
allele num: 118838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+25A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+25A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+25A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+25A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+25A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+25A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+25A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+25A>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8697
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

10-7627850-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627850
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627850
    reference: chr 10
allele count: 1
allele frequency: 8.353939717970996e-6
allele num: 119704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+14C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+14C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+14C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+14C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+14C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+14C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+14C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+14C>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8804
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 891
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

10-7627850-GGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627850
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627848
    reference: chr 10
allele count: 1
allele frequency: 8.353939717970996e-6
allele num: 119704
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108+12_1108+13delAC
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108+12_1108+13delAC
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733+12_733+13delAC
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651+12_5651+13delAC
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466+12_466+13delAC
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194+12_*194+13delAC
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454+12_454+13delAC
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108+12_1108+13delAC
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20295
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41969
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: GGT
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

10-7627864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627864
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627864
    reference: chr 10
allele count: 1
allele frequency: 8.29242404139578e-6
allele num: 120592
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*194G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1108G>A
  hgvsp: ENSP00000380333.2:p.Gly370Ser
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1108G>A
  hgvsp: ENSP00000256861.6:p.Gly370Ser
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.733G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5651G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.466G>A
  hgvsp: ENSP00000298441.6:p.Gly156Ser
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.454G>A
  hgvsp: ENSP00000387969.2:p.Gly152Ser
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1108G>A
  hgvsp: ENSP00000380332.2:p.Gly370Ser
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8859
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2149
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly370Ser
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

10-7627879-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627879
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627879
    reference: chr 10
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.451A>T
  hgvsp: ENSP00000298441.6:p.Met151Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.718A>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5636A>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1093A>T
  hgvsp: ENSP00000256861.6:p.Met365Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1093A>T
  hgvsp: ENSP00000380332.2:p.Met365Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.439A>T
  hgvsp: ENSP00000387969.2:p.Met147Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1093A>T
  hgvsp: ENSP00000380333.2:p.Met365Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*179A>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8867
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Met365Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

10-7627881-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627881
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627881
    reference: chr 10
allele count: 45
allele frequency: 3.714526274082512e-4
allele num: 121146
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1091A>G
  hgvsp: ENSP00000256861.6:p.His364Arg
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5634A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.437A>G
  hgvsp: ENSP00000387969.2:p.His146Arg
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.716A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1091A>G
  hgvsp: ENSP00000380333.2:p.His364Arg
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1091A>G
  hgvsp: ENSP00000380332.2:p.His364Arg
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*177A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.449A>G
  hgvsp: ENSP00000298441.6:p.His150Arg
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 20893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 947
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2148
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His364Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

10-7627891-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627891
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627891
    reference: chr 10
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1081T>C
  hgvsp: ENSP00000380333.2:p.Tyr361His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1081T>C
  hgvsp: ENSP00000256861.6:p.Tyr361His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.439T>C
  hgvsp: ENSP00000298441.6:p.Tyr147His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.706T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5624T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1081T>C
  hgvsp: ENSP00000380332.2:p.Tyr361His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*167T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.427T>C
  hgvsp: ENSP00000387969.2:p.Tyr143His
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8895
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8886
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43461
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1818
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Tyr361His
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

10-7627893-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627893
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627893
    reference: chr 10
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5622T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*165T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.425T>C
  hgvsp: ENSP00000387969.2:p.Val142Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1079T>C
  hgvsp: ENSP00000380333.2:p.Val360Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1079T>C
  hgvsp: ENSP00000256861.6:p.Val360Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1079T>C
  hgvsp: ENSP00000380332.2:p.Val360Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.437T>C
  hgvsp: ENSP00000298441.6:p.Val146Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.704T>C
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val360Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

10-7627906-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627906
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627906
    reference: chr 10
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*152A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1066A>G
  hgvsp: ENSP00000380333.2:p.Arg356Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.412A>G
  hgvsp: ENSP00000387969.2:p.Arg138Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1066A>G
  hgvsp: ENSP00000256861.6:p.Arg356Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1066A>G
  hgvsp: ENSP00000380332.2:p.Arg356Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.691A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.424A>G
  hgvsp: ENSP00000298441.6:p.Arg142Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5609A>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25361
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8894
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg356Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

10-7627910-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627910
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627910
    reference: chr 10
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1062C>T
  hgvsp: ENST00000397146.2:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.420C>T
  hgvsp: ENST00000298441.6:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1062C>T
  hgvsp: ENST00000256861.6:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.408C>T
  hgvsp: ENST00000446830.2:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.687C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5605C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1062C>T
  hgvsp: ENST00000397145.2:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*148C>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1821
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser354Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-7627911-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627911
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627911
    reference: chr 10
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1061G>A
  hgvsp: ENSP00000256861.6:p.Ser354Asn
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1061G>A
  hgvsp: ENSP00000380333.2:p.Ser354Asn
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.686G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1061G>A
  hgvsp: ENSP00000380332.2:p.Ser354Asn
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.407G>A
  hgvsp: ENSP00000387969.2:p.Ser136Asn
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*147G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5604G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.419G>A
  hgvsp: ENSP00000298441.6:p.Ser140Asn
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8898
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser354Asn
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum

10-7627912-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627912
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627912
    reference: chr 10
allele count: 8
allele frequency: 6.591957811470006e-5
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1060A>G
  hgvsp: ENSP00000380333.2:p.Ser354Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1060A>G
  hgvsp: ENSP00000256861.6:p.Ser354Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1060A>G
  hgvsp: ENSP00000380332.2:p.Ser354Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*146A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.406A>G
  hgvsp: ENSP00000387969.2:p.Ser136Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5603A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.685A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.418A>G
  hgvsp: ENSP00000298441.6:p.Ser140Gly
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25370
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8914
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser354Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/10-7627927-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627927
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627927
    reference: chr 10
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1045T>G
  hgvsp: ENSP00000256861.6:p.Ser349Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*131T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1045T>G
  hgvsp: ENSP00000380332.2:p.Ser349Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.391T>G
  hgvsp: ENSP00000387969.2:p.Ser131Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.670T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1045T>G
  hgvsp: ENSP00000380333.2:p.Ser349Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5588T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.403T>G
  hgvsp: ENSP00000298441.6:p.Ser135Ala
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser349Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

10-7627936-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627936
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627936
    reference: chr 10
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.661C>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5579C>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1036C>A
  hgvsp: ENSP00000256861.6:p.His346Asn
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1036C>A
  hgvsp: ENSP00000380333.2:p.His346Asn
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*122C>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1036C>A
  hgvsp: ENSP00000380332.2:p.His346Asn
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.382C>A
  hgvsp: ENSP00000387969.2:p.His128Asn
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.394C>A
  hgvsp: ENSP00000298441.6:p.His132Asn
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8901
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1820
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His346Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS

10-7627937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627937
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627937
    reference: chr 10
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1035C>T
  hgvsp: ENST00000256861.6:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.660C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.393C>T
  hgvsp: ENST00000298441.6:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1035C>T
  hgvsp: ENST00000397146.2:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5578C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.381C>T
  hgvsp: ENST00000446830.2:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1035C>T
  hgvsp: ENST00000397145.2:c.1035C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*121C>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1819
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8900
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp345Asp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

10-7627938-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627938
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627938
    reference: chr 10
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1034A>C
  hgvsp: ENSP00000256861.6:p.Asp345Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*120A>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.659A>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1034A>C
  hgvsp: ENSP00000380332.2:p.Asp345Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.392A>C
  hgvsp: ENSP00000298441.6:p.Asp131Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5577A>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1034A>C
  hgvsp: ENSP00000380333.2:p.Asp345Ala
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.380A>C
  hgvsp: ENSP00000387969.2:p.Asp127Ala
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 945
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8901
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp345Ala
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-7627945-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627945
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627945
    reference: chr 10
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*113T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.385T>G
  hgvsp: ENSP00000298441.6:p.Trp129Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.652T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1027T>G
  hgvsp: ENSP00000380332.2:p.Trp343Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1027T>G
  hgvsp: ENSP00000380333.2:p.Trp343Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5570T>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.373T>G
  hgvsp: ENSP00000387969.2:p.Trp125Gly
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1027T>G
  hgvsp: ENSP00000256861.6:p.Trp343Gly
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8915
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1815
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Trp343Gly
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

10-7627946-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627946
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627946
    reference: chr 10
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.384A>G
  hgvsp: ENST00000298441.6:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5569A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*112A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1026A>G
  hgvsp: ENST00000397146.2:c.1026A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.372A>G
  hgvsp: ENST00000446830.2:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1026A>G
  hgvsp: ENST00000256861.6:c.1026A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.651A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1026A>G
  hgvsp: ENST00000397145.2:c.1026A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 942
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43601
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val342Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum

10-7627956-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627956
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627956
    reference: chr 10
allele count: 4
allele frequency: 3.296033224014898e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5559G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1016G>A
  hgvsp: ENSP00000380333.2:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1016G>A
  hgvsp: ENSP00000256861.6:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.374G>A
  hgvsp: ENSP00000298441.6:p.Arg125Gln
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.362G>A
  hgvsp: ENSP00000387969.2:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1016G>A
  hgvsp: ENSP00000380332.2:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*102G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.641G>A
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg339Gln
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-7627957-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627957
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627957
    reference: chr 10
allele count: 185
allele frequency: 1.524365122525997e-3
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1015C>T
  hgvsp: ENSP00000380333.2:p.Arg339Trp
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1015C>T
  hgvsp: ENSP00000256861.6:p.Arg339Trp
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1015C>T
  hgvsp: ENSP00000380332.2:p.Arg339Trp
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.640C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*101C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5558C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.361C>T
  hgvsp: ENSP00000387969.2:p.Arg121Trp
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.373C>T
  hgvsp: ENSP00000298441.6:p.Arg125Trp
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 25406
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 8911
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20648
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43486
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg339Trp
num of homozygotes: 2
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

10-7627958-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627958
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627958
    reference: chr 10
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1014C>G
  hgvsp: ENSP00000256861.6:p.Asn338Lys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.360C>G
  hgvsp: ENSP00000387969.2:p.Asn120Lys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.639C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.372C>G
  hgvsp: ENSP00000298441.6:p.Asn124Lys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1014C>G
  hgvsp: ENSP00000380333.2:p.Asn338Lys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1014C>G
  hgvsp: ENSP00000380332.2:p.Asn338Lys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*100C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5557C>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43620
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2133
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn338Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

10-7627971-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627971
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627971
    reference: chr 10
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1001T>C
  hgvsp: ENSP00000256861.6:p.Ile334Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5544T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1001T>C
  hgvsp: ENSP00000380332.2:p.Ile334Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.626T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*87T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.347T>C
  hgvsp: ENSP00000387969.2:p.Ile116Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1001T>C
  hgvsp: ENSP00000380333.2:p.Ile334Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.359T>C
  hgvsp: ENSP00000298441.6:p.Ile120Thr
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile334Thr
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-7627972-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627972
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627972
    reference: chr 10
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*86A>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1000A>T
  hgvsp: ENSP00000380333.2:p.Ile334Phe
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.346A>T
  hgvsp: ENSP00000387969.2:p.Ile116Phe
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.358A>T
  hgvsp: ENSP00000298441.6:p.Ile120Phe
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5543A>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1000A>T
  hgvsp: ENSP00000256861.6:p.Ile334Phe
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1000A>T
  hgvsp: ENSP00000380332.2:p.Ile334Phe
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.625A>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43585
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8879
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile334Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

10-7627972-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627972
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627972
    reference: chr 10
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*86A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.1000A>G
  hgvsp: ENSP00000380332.2:p.Ile334Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.625A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.346A>G
  hgvsp: ENSP00000387969.2:p.Ile116Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.358A>G
  hgvsp: ENSP00000298441.6:p.Ile120Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5543A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.1000A>G
  hgvsp: ENSP00000380333.2:p.Ile334Val
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.1000A>G
  hgvsp: ENSP00000256861.6:p.Ile334Val
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20609
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile334Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

10-7627983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627983
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627983
    reference: chr 10
allele count: 10
allele frequency: 8.248783304462591e-5
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.989G>A
  hgvsp: ENSP00000380332.2:p.Arg330His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.347G>A
  hgvsp: ENSP00000298441.6:p.Arg116His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.989G>A
  hgvsp: ENSP00000380333.2:p.Arg330His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.989G>A
  hgvsp: ENSP00000256861.6:p.Arg330His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5532G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*75G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.335G>A
  hgvsp: ENSP00000387969.2:p.Arg112His
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.614G>A
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8950
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43399
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2108
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg330His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ

10-7627984-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627984
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627984
    reference: chr 10
allele count: 6
allele frequency: 4.950249987624375e-5
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.988C>T
  hgvsp: ENSP00000256861.6:p.Arg330Cys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.988C>T
  hgvsp: ENSP00000380332.2:p.Arg330Cys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.613C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.334C>T
  hgvsp: ENSP00000387969.2:p.Arg112Cys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5531C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.988C>T
  hgvsp: ENSP00000380333.2:p.Arg330Cys
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.346C>T
  hgvsp: ENSP00000298441.6:p.Arg116Cys
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg330Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

10-7627991-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627991
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627991
    reference: chr 10
allele count: 5
allele frequency: 4.128955539406752e-5
allele num: 121096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.606C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.339C>T
  hgvsp: ENST00000298441.6:c.339C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.327C>T
  hgvsp: ENST00000446830.2:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5524C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*67C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.981C>T
  hgvsp: ENST00000397146.2:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.981C>T
  hgvsp: ENST00000397145.2:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.981C>T
  hgvsp: ENST00000256861.6:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8925
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43246
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro327Pro
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

10-7627992-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627992
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627992
    reference: chr 10
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5523C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.326C>T
  hgvsp: ENSP00000387969.2:p.Pro109Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.980C>T
  hgvsp: ENSP00000380333.2:p.Pro327Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*66C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.605C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.980C>T
  hgvsp: ENSP00000256861.6:p.Pro327Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.980C>T
  hgvsp: ENSP00000380332.2:p.Pro327Leu
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.338C>T
  hgvsp: ENSP00000298441.6:p.Pro113Leu
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8795
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43131
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro327Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

10-7627994-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627994
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627994
    reference: chr 10
allele count: 3
allele frequency: 2.480240748702007e-5
allele num: 120956
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.978A>G
  hgvsp: ENST00000397145.2:c.978A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.603A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.978A>G
  hgvsp: ENST00000256861.6:c.978A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*64A>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.978A>G
  hgvsp: ENST00000397146.2:c.978A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.324A>G
  hgvsp: ENST00000446830.2:c.324A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.336A>G
  hgvsp: ENST00000298441.6:c.336A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5521A>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8911
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg326Arg
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

10-7627996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7627996
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7627996
    reference: chr 10
allele count: 4
allele frequency: 3.311148637462336e-5
allele num: 120804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.334C>T
  hgvsp: ENSP00000298441.6:p.Arg112Ter
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*62C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.976C>T
  hgvsp: ENSP00000256861.6:p.Arg326Ter
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.976C>T
  hgvsp: ENSP00000380332.2:p.Arg326Ter
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.322C>T
  hgvsp: ENSP00000387969.2:p.Arg108Ter
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.976C>T
  hgvsp: ENSP00000380333.2:p.Arg326Ter
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5519C>T
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.601C>T
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20011
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8924
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42656
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg326Ter
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

10-7628003-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7628003
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7628003
    reference: chr 10
allele count: 1
allele frequency: 8.289811821271656e-6
allele num: 120630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.315T>C
  hgvsp: ENST00000446830.2:c.315T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.969T>C
  hgvsp: ENST00000397146.2:c.969T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.969T>C
  hgvsp: ENST00000256861.6:c.969T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.969T>C
  hgvsp: ENST00000397145.2:c.969T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.594T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*55T>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.327T>C
  hgvsp: ENST00000298441.6:c.327T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5512T>C
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8868
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42725
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His323His
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

10-7628006-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7628006
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7628006
    reference: chr 10
allele count: 1
allele frequency: 8.301510874979247e-6
allele num: 120460
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.966C>G
  hgvsp: ENST00000256861.6:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.324C>G
  hgvsp: ENST00000298441.6:c.324C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.966C>G
  hgvsp: ENST00000397146.2:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*52C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.312C>G
  hgvsp: ENST00000446830.2:c.312C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.591C>G
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.966C>G
  hgvsp: ENST00000397145.2:c.966C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5509C>G
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8643
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42394
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1743
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu322Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

10-7628014-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7628014
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7628014
    reference: chr 10
allele count: 1
allele frequency: 8.331111703545721e-6
allele num: 120032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.304A>C
  hgvsp: ENSP00000387969.2:p.Thr102Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.958A>C
  hgvsp: ENSP00000380332.2:p.Thr320Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.583A>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.316A>C
  hgvsp: ENSP00000298441.6:p.Thr106Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*44A>C
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.958A>C
  hgvsp: ENSP00000256861.6:p.Thr320Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.958A>C
  hgvsp: ENSP00000380333.2:p.Thr320Pro
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5501A>C
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8534
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr320Pro
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

10-7628023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 7628023
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 7628023
    reference: chr 10
allele count: 1
allele frequency: 8.409438754057554e-6
allele num: 118914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380333
  ensembl transcript: ENST00000397146
  gene symbol: ITIH5
  hgvsc: ENST00000397146.2:c.949G>A
  hgvsp: ENSP00000380333.2:p.Ala317Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000434980
  gene symbol: ITIH5
  hgvsc: ENST00000434980.1:n.574G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000380332
  ensembl transcript: ENST00000397145
  gene symbol: ITIH5
  hgvsc: ENST00000397145.2:c.949G>A
  hgvsp: ENSP00000380332.2:p.Ala317Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000419386
  ensembl transcript: ENST00000461751
  gene symbol: ITIH5
  hgvsc: ENST00000461751.1:c.*35G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000123243
  ensembl transcript: ENST00000476417
  gene symbol: ITIH5
  hgvsc: ENST00000476417.1:n.5492G>A
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000387969
  ensembl transcript: ENST00000446830
  gene symbol: ITIH5
  hgvsc: ENST00000446830.2:c.295G>A
  hgvsp: ENSP00000387969.2:p.Ala99Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000298441
  ensembl transcript: ENST00000298441
  gene symbol: ITIH5
  hgvsc: ENST00000298441.6:c.307G>A
  hgvsp: ENSP00000298441.6:p.Ala103Thr
  variant of: http://identifiers.org/hgnc/21449
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000123243
  ensembl protein: ENSP00000256861
  ensembl transcript: ENST00000256861
  gene symbol: ITIH5
  hgvsc: ENST00000256861.6:c.949G>A
  hgvsp: ENSP00000256861.6:p.Ala317Thr
  variant of: http://identifiers.org/hgnc/21449
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18079
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala317Thr
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 294
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19764
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3009
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21755
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8926
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.178411501296253e-4
allele num: 8486
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55996
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

DP
type: SiteQuality
SIO_000300: 1.14417e6

QD
type: SiteQuality
SIO_000300: 2.73e0

VQSLOD
type: SiteQuality
SIO_000300: -3.244e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.312e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

GenotypeQuality
all individuals: 17513
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1051
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 370
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.840739240879137e-5
allele num: 54326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.145e0

QD
type: SiteQuality
SIO_000300: 7.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.082818e6

VQSLOD
type: SiteQuality
SIO_000300: -9.685e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 919
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 566
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17513
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 724
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.840739240879137e-5
allele num: 54326
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14202
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

DP
type: SiteQuality
SIO_000300: 1.082818e6

MQRankSum
type: SiteQuality
SIO_000300: -1.145e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -9.685e-1

QD
type: SiteQuality
SIO_000300: 7.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 969
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13930
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1212
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1038
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4680
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53114
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.425418384671356e-4
allele num: 8246
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14038
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4488
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.275e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.79e-1

DP
type: SiteQuality
SIO_000300: 1.033107e6

GenotypeQuality
all individuals: 501
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2903
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4528
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11417
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5018
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1726
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23730
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7756
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13788
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.271294177472667e-4
allele num: 7866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51546
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5784
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.82e0

VQSLOD
type: SiteQuality
SIO_000300: -2.76e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

MQRankSum
type: SiteQuality
SIO_000300: 2.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

QD
type: SiteQuality
SIO_000300: 1.901e1

DP
type: SiteQuality
SIO_000300: 9.86714e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

GenotypeQuality
all individuals: 11779
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2866
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23928
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4505
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13784
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.939337522302381e-5
allele num: 51564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7722
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

DP
type: SiteQuality
SIO_000300: 9.85625e5

BaseQRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: -1.883e0

QD
type: SiteQuality
SIO_000300: 2.835e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.622e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.69e-1

GenotypeQuality
all individuals: 1574
bin: 6.75e1
variant carriers: 139

GenotypeQuality
all individuals: 661
bin: 5.25e1
variant carriers: 113

GenotypeQuality
all individuals: 1792
bin: 7.5e0
variant carriers: 33

GenotypeQuality
all individuals: 892
bin: 1.75e1
variant carriers: 63

GenotypeQuality
all individuals: 494
bin: 4.25e1
variant carriers: 84

GenotypeQuality
all individuals: 523
bin: 4.75e1
variant carriers: 112

GenotypeQuality
all individuals: 3746
bin: 2.75e1
variant carriers: 60

GenotypeQuality
all individuals: 22448
bin: 2.25e1
variant carriers: 71

GenotypeQuality
all individuals: 246
bin: 8.75e1
variant carriers: 167

GenotypeQuality
all individuals: 8841
bin: 9.75e1
variant carriers: 8491

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 150

GenotypeQuality
all individuals: 487
bin: 7.75e1
variant carriers: 143

GenotypeQuality
all individuals: 450
bin: 7.25e1
variant carriers: 114

European (Non-Finnish)
type: Population
allele count: 6451
allele frequency: 1.271433639481257e-1
allele num: 50738
num of homozygotes: 317

East Asian
type: Population
allele count: 57
allele frequency: 9.916492693110648e-3
allele num: 5748
num of homozygotes: 1

South Asian
type: Population
allele count: 1357
allele frequency: 9.897884755652808e-2
allele num: 13710
num of homozygotes: 68

Other
type: Population
allele count: 63
allele frequency: 9.402985074626866e-2
allele num: 670
num of homozygotes: 1

African
type: Population
allele count: 225
allele frequency: 2.936570086139389e-2
allele num: 7662
num of homozygotes: 4

Latino
type: Population
allele count: 1106
allele frequency: 1.450301599790191e-1
allele num: 7626
num of homozygotes: 54

European (Finnish)
type: Population
allele count: 711
allele frequency: 1.702586206896552e-1
allele num: 4176
num of homozygotes: 51

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.68e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

QD
type: SiteQuality
SIO_000300: 1.341e1

DP
type: SiteQuality
SIO_000300: 9.75039e5

MQRankSum
type: SiteQuality
SIO_000300: 9.4e-2

GenotypeQuality
all individuals: 1836
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28098
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4520
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 482
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 926
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 260
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 442
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3794
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7544
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.076756936368168e-5
allele num: 48152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6964
num of homozygotes: 0

South Asian
type: Population
allele count: 21
allele frequency: 1.573976915005247e-3
allele num: 13342
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.3e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.070000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.00179e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.8e-3

FS
type: SiteQuality
SIO_000300: 1.037e0

QD
type: SiteQuality
SIO_000300: 1.248e1

GenotypeQuality
all individuals: 350
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1046
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9742
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4806
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.163846453455663e-5
allele num: 46214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3510
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.383125864453665e-4
allele num: 7230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5314
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13030
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

QD
type: SiteQuality
SIO_000300: 1.287e1

VQSLOD
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.922e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

FS
type: SiteQuality
SIO_000300: 8.654999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.516e0

DP
type: SiteQuality
SIO_000300: 8.53554e5

GenotypeQuality
all individuals: 147
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1495
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3219
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10204
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28510
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4811
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13078
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5360
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.150722642807983e-5
allele num: 46496
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

MQ
type: SiteQuality
SIO_000300: 5.936e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 8.50363e5

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

QD
type: SiteQuality
SIO_000300: 1.436e1

GenotypeQuality
all individuals: 5008
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27458
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8218
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5221
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 542
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7042
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.217589923271389e-5
allele num: 45094
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

QD
type: SiteQuality
SIO_000300: 8.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.19319e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

GenotypeQuality
all individuals: 5474
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5606
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1936
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3064
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4694
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.338634237605238e-5
allele num: 42760
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.206e1

VQSLOD
type: SiteQuality
SIO_000300: 6.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

DP
type: SiteQuality
SIO_000300: 7.78524e5

FS
type: SiteQuality
SIO_000300: 6.345e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.65e-1

GenotypeQuality
all individuals: 7564
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3968
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20659
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1081
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4778
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2480
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 488
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.3206e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.481e1

MQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.59e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

VQSLOD
type: SiteQuality
SIO_000300: 2.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.734e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1877
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9153
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7470
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 13965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4614
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.952465308532625e-5
allele num: 33870
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1856
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3664
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

DP
type: SiteQuality
SIO_000300: 7.10949e5

QD
type: SiteQuality
SIO_000300: 5.71e0

FS
type: SiteQuality
SIO_000300: 1.856e0

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.539e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.03e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7470
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 1244
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1735
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3216
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9153
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33870
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.931247585940518e-4
allele num: 5178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1856
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.180661577608143e-4
allele num: 3144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11236
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.856e0

QD
type: SiteQuality
SIO_000300: 5.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 7.10949e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.03e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.539e0

GenotypeQuality
all individuals: 4815
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4986
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1245
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1671
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 835
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7344
bin: 1.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5562
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.119e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.78e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 7.15672e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.107e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3307
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 15503
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7398
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1246
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5806
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 5.717552887364208e-4
allele num: 3498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4112
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

FS
type: SiteQuality
SIO_000300: 1.821e0

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

QD
type: SiteQuality
SIO_000300: 9.199999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.16062e5

GenotypeQuality
all individuals: 8141
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2093
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6963
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6294
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1562
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2243
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4317
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2068
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11918
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.705481305124182e-5
allele num: 36962
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.46e-1

DP
type: SiteQuality
SIO_000300: 7.34607e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.129e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 5.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.137e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e-1

GenotypeQuality
all individuals: 5270
bin: 3.75e1
variant carriers: 5250

GenotypeQuality
all individuals: 4317
bin: 2.75e1
variant carriers: 4271

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 658

GenotypeQuality
all individuals: 6963
bin: 3.25e1
variant carriers: 6918

GenotypeQuality
all individuals: 823
bin: 8.25e1
variant carriers: 819

GenotypeQuality
all individuals: 8576
bin: 2.25e1
variant carriers: 8123

GenotypeQuality
all individuals: 2068
bin: 4.25e1
variant carriers: 2063

GenotypeQuality
all individuals: 8141
bin: 9.75e1
variant carriers: 8134

GenotypeQuality
all individuals: 2865
bin: 4.75e1
variant carriers: 2861

GenotypeQuality
all individuals: 678
bin: 9.25e1
variant carriers: 678

GenotypeQuality
all individuals: 557
bin: 7.25e1
variant carriers: 555

GenotypeQuality
all individuals: 1084
bin: 6.75e1
variant carriers: 1068

African
type: Population
allele count: 4437
allele frequency: 7.708478109798471e-1
allele num: 5756
num of homozygotes: 1684

European (Non-Finnish)
type: Population
allele count: 32846
allele frequency: 8.886423894810886e-1
allele num: 36962
num of homozygotes: 14562

South Asian
type: Population
allele count: 10111
allele frequency: 8.483806007719416e-1
allele num: 11918
num of homozygotes: 4281

Latino
type: Population
allele count: 4198
allele frequency: 9.399910434393193e-1
allele num: 4466
num of homozygotes: 1971

Other
type: Population
allele count: 403
allele frequency: 8.799126637554585e-1
allele num: 458
num of homozygotes: 177

East Asian
type: Population
allele count: 3816
allele frequency: 9.994761655316919e-1
allele num: 3818
num of homozygotes: 1907

European (Finnish)
type: Population
allele count: 2140
allele frequency: 9.083191850594228e-1
allele num: 2356
num of homozygotes: 964

DP
type: SiteQuality
SIO_000300: 7.34607e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 1.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 3.137e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e0

GenotypeQuality
all individuals: 80
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2716
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5382
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 16342
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 51
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 367
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1931
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 311
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1676
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3684
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 2.921129503407984e-4
allele num: 20540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.160092807424594e-3
allele num: 862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8864
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.705e1

MQRankSum
type: SiteQuality
SIO_000300: -5.05e-1

QD
type: SiteQuality
SIO_000300: 8.100000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.54e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.028e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.029e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

FS
type: SiteQuality
SIO_000300: 2.0781e1

DP
type: SiteQuality
SIO_000300: 5.28462e5

GenotypeQuality
all individuals: 373
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3101
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1752
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1230
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8828
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

QD
type: SiteQuality
SIO_000300: 2.45e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.29008e5

MQ
type: SiteQuality
SIO_000300: 5.739e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.92e-2

GenotypeQuality
all individuals: 2982
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 385
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20485
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17544
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1590
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20898
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.17598e5

QD
type: SiteQuality
SIO_000300: 2.965e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.03e-2

GenotypeQuality
all individuals: 637
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 207
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 114
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 96
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 10729
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10650
bin: 1.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 82
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7473
bin: 1.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1328
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 5.637982195845697e-3
allele num: 3370
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7634
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.468e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 8.964e0

VQSLOD
type: SiteQuality
SIO_000300: 4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.85e-2

DP
type: SiteQuality
SIO_000300: 5.01787e5

GenotypeQuality
all individuals: 4096
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4740
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5478
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2612
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1588
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19894
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.266e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 5.17645e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.99e0

GenotypeQuality
all individuals: 629
bin: 5.75e1
variant carriers: 627

GenotypeQuality
all individuals: 1230
bin: 5.25e1
variant carriers: 1222

GenotypeQuality
all individuals: 382
bin: 8.25e1
variant carriers: 382

GenotypeQuality
all individuals: 407
bin: 8.75e1
variant carriers: 406

GenotypeQuality
all individuals: 9113
bin: 2.25e1
variant carriers: 8867

GenotypeQuality
all individuals: 4740
bin: 3.25e1
variant carriers: 4680

GenotypeQuality
all individuals: 519
bin: 9.25e1
variant carriers: 519

GenotypeQuality
all individuals: 311
bin: 7.25e1
variant carriers: 311

GenotypeQuality
all individuals: 1588
bin: 4.75e1
variant carriers: 1569

GenotypeQuality
all individuals: 621
bin: 6.75e1
variant carriers: 610

GenotypeQuality
all individuals: 886
bin: 6.25e1
variant carriers: 876

GenotypeQuality
all individuals: 386
bin: 7.75e1
variant carriers: 385

East Asian
type: Population
allele count: 1628
allele frequency: 9.987730061349693e-1
allele num: 1630
num of homozygotes: 813

South Asian
type: Population
allele count: 6998
allele frequency: 8.413080067323876e-1
allele num: 8318
num of homozygotes: 2952

European (Non-Finnish)
type: Population
allele count: 17566
allele frequency: 8.829797929023826e-1
allele num: 19894
num of homozygotes: 7745

European (Finnish)
type: Population
allele count: 1176
allele frequency: 9.004594180704441e-1
allele num: 1306
num of homozygotes: 526

African
type: Population
allele count: 2854
allele frequency: 7.639186295503212e-1
allele num: 3736
num of homozygotes: 1079

Other
type: Population
allele count: 270
allele frequency: 8.653846153846154e-1
allele num: 312
num of homozygotes: 117

Latino
type: Population
allele count: 1422
allele frequency: 9.2578125e-1
allele num: 1536
num of homozygotes: 658

DP
type: SiteQuality
SIO_000300: 5.17645e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.99e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 3.266e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

GenotypeQuality
all individuals: 1872
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1569
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3658
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2943
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11903
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2683
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2176
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7429
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2620
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 838
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.580677794638341e-5
allele num: 63264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12480
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.436e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

FS
type: SiteQuality
SIO_000300: 6.78e0

QD
type: SiteQuality
SIO_000300: 3.57e0

DP
type: SiteQuality
SIO_000300: 1.786694e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.659e0

MQ
type: SiteQuality
SIO_000300: 6.004e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.01e-1

GenotypeQuality
all individuals: 8023
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2443
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6611
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1882
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2014
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1426
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16021
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2634
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2659
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13184
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.135722174499939e-5
allele num: 65192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.359e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQ
type: SiteQuality
SIO_000300: 5.863e1

DP
type: SiteQuality
SIO_000300: 1.777667e6

VQSLOD
type: SiteQuality
SIO_000300: -1.869e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.85e-1

FS
type: SiteQuality
SIO_000300: 3.023e0

GenotypeQuality
all individuals: 2629
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17099
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1390
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8017
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2420
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6615
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.191043353978085e-4
allele num: 8396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.68521364893944e-5
allele num: 13012
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.158583525789069e-5
allele num: 64950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

VQSLOD
type: SiteQuality
SIO_000300: 4.22e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

MQ
type: SiteQuality
SIO_000300: 5.889e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.77827e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

GenotypeQuality
all individuals: 3492
bin: 2.25e1
variant carriers: 39

GenotypeQuality
all individuals: 2357
bin: 7.5e0
variant carriers: 43

GenotypeQuality
all individuals: 2812
bin: 2.75e1
variant carriers: 38

GenotypeQuality
all individuals: 2509
bin: 1.75e1
variant carriers: 36

GenotypeQuality
all individuals: 331
bin: 8.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2532
bin: 4.75e1
variant carriers: 20

GenotypeQuality
all individuals: 196
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 216
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2436
bin: 6.75e1
variant carriers: 11

GenotypeQuality
all individuals: 1024
bin: 9.75e1
variant carriers: 63

GenotypeQuality
all individuals: 1739
bin: 5.75e1
variant carriers: 20

GenotypeQuality
all individuals: 583
bin: 7.75e1
variant carriers: 8

African
type: Population
allele count: 35
allele frequency: 5.165289256198347e-3
allele num: 6776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 32
allele frequency: 9.024252679075015e-3
allele num: 3546
num of homozygotes: 0

South Asian
type: Population
allele count: 22
allele frequency: 3.603013429413692e-3
allele num: 6106
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 1.229508196721311e-2
allele num: 488
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 4.379341588643914e-3
allele num: 6622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 185
allele frequency: 4.420127108520093e-3
allele num: 41854
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.872659176029963e-3
allele num: 5340
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.122e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.34e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

FS
type: SiteQuality
SIO_000300: 1.327e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.51e-2

DP
type: SiteQuality
SIO_000300: 1.679592e6

QD
type: SiteQuality
SIO_000300: 1.13e0

GenotypeQuality
all individuals: 513
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25811
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7444
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1219
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547556408431087e-5
allele num: 64618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.813e1

FS
type: SiteQuality
SIO_000300: 4.322e0

VQSLOD
type: SiteQuality
SIO_000300: -1.322e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.43e0

DP
type: SiteQuality
SIO_000300: 1.57926e6

QD
type: SiteQuality
SIO_000300: 3.53e0

MQRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.182e0

GenotypeQuality
all individuals: 25811
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2064
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3235
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7444
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12516
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.57926e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e0

MQ
type: SiteQuality
SIO_000300: 5.813e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.182e0

FS
type: SiteQuality
SIO_000300: 4.322e0

VQSLOD
type: SiteQuality
SIO_000300: -1.322e0

QD
type: SiteQuality
SIO_000300: 3.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.43e0

GenotypeQuality
all individuals: 1760
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2038
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6916
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1776
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2822
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 28922
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 942
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1547
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 468
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1662
bin: 7.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.676659528907923e-4
allele num: 11208
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.192179303767287e-4
allele num: 8388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.29489291598023e-4
allele num: 6070
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.67000668002672e-4
allele num: 11976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.404319061290725e-4
allele num: 64088
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.445e0

DP
type: SiteQuality
SIO_000300: 1.605496e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.074e0

VQSLOD
type: SiteQuality
SIO_000300: -2.717e0

MQRankSum
type: SiteQuality
SIO_000300: -1.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.100000000000001e-1

QD
type: SiteQuality
SIO_000300: 4.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.49e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

GenotypeQuality
all individuals: 166
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2396
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1664
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34210
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1839
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.94325689856199e-4
allele num: 10292
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13224
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

VQSLOD
type: SiteQuality
SIO_000300: -8.06e-1

DP
type: SiteQuality
SIO_000300: 1.608749e6

FS
type: SiteQuality
SIO_000300: 2.244e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

QD
type: SiteQuality
SIO_000300: 1.566e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

MQ
type: SiteQuality
SIO_000300: 5.478e1

GenotypeQuality
all individuals: 732
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39341
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1818
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.254788160185723e-5
allele num: 13784
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 11488
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65740
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.617e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -2.338e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 5.824e1

QD
type: SiteQuality
SIO_000300: 6.19e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

DP
type: SiteQuality
SIO_000300: 1.644634e6

GenotypeQuality
all individuals: 2322
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40176
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8627
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 8.75e1
variant carriers: 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: 8632
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14128
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: 8.699999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 5.705e1

FS
type: SiteQuality
SIO_000300: 3.769e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 1.652051e6

QD
type: SiteQuality
SIO_000300: 1.622e1

VQSLOD
type: SiteQuality
SIO_000300: -1.107e-1

GenotypeQuality
all individuals: 463
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40680
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 464
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14442
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515702679762338e-5
allele num: 65976
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.54e-1

FS
type: SiteQuality
SIO_000300: 1.289e0

DP
type: SiteQuality
SIO_000300: 1.660756e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 3.467e1

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41008
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2134
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2309
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1830
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14660
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51372952680815e-5
allele num: 66062
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.24e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

MQRankSum
type: SiteQuality
SIO_000300: -6.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.56e-1

QD
type: SiteQuality
SIO_000300: 1.407e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

FS
type: SiteQuality
SIO_000300: 2.53e0

DP
type: SiteQuality
SIO_000300: 1.663772e6

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 415
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1833
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2137
bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14718
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: 4
allele frequency: 6.054368226675546e-5
allele num: 66068
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

FS
type: SiteQuality
SIO_000300: 2.443e0

DP
type: SiteQuality
SIO_000300: 1.665127e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

QD
type: SiteQuality
SIO_000300: 1.437e1

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8764
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2332
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2146
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41969
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1826
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66264
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: 8650
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.161e0

DP
type: SiteQuality
SIO_000300: 1.676324e6

QD
type: SiteQuality
SIO_000300: 1.575e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.662e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 5.841e1

FS
type: SiteQuality
SIO_000300: 2.249e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8764
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2332
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 462
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1826
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509115054931788e-5
allele num: 66264
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.676324e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.161e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.662e0

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 2.249e0

QD
type: SiteQuality
SIO_000300: 1.575e1

MQ
type: SiteQuality
SIO_000300: 5.841e1

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42768
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8813
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2298
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.2625250501002e-5
allele num: 15968
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.687727e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.983e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.268e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.478e1

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

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

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

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 454
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2297
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43320
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.296e0

FS
type: SiteQuality
SIO_000300: 2.111e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.25e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.73e-1

QD
type: SiteQuality
SIO_000300: 1.186e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

MQRankSum
type: SiteQuality
SIO_000300: -1.011e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.05e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

DP
type: SiteQuality
SIO_000300: 1.695192e6

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

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

GenotypeQuality
all individuals: 8866
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1821
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2335
bin: 9.75e1
variant carriers: 45

GenotypeQuality
all individuals: 43357
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 45
allele frequency: 3.888024883359254e-3
allele num: 11574
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.276e1

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

DP
type: SiteQuality
SIO_000300: 1.698385e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

MQ
type: SiteQuality
SIO_000300: 5.891e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.11e-1

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2292
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 452
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 947
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.435e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 6.352e0

QD
type: SiteQuality
SIO_000300: 1.221e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

DP
type: SiteQuality
SIO_000300: 1.697375e6

MQRankSum
type: SiteQuality
SIO_000300: 7.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

GenotypeQuality
all individuals: 81
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2145
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1821
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43488
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8887
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2292
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

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

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

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

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

FS
type: SiteQuality
SIO_000300: 4.312e0

VQSLOD
type: SiteQuality
SIO_000300: -3.783e0

MQ
type: SiteQuality
SIO_000300: 5.868e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-1

QD
type: SiteQuality
SIO_000300: 1.141e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.4e0

MQRankSum
type: SiteQuality
SIO_000300: -1.846e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.399e0

DP
type: SiteQuality
SIO_000300: 1.697846e6

GenotypeQuality
all individuals: 2141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43584
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 945
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.212268153715602e-4
allele num: 16498
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.048e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.903e1

DP
type: SiteQuality
SIO_000300: 1.699476e6

QD
type: SiteQuality
SIO_000300: 1.11e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.38e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-2

GenotypeQuality
all individuals: 43607
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8898
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: 8.64e-1

FS
type: SiteQuality
SIO_000300: 4.426e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.352e1

DP
type: SiteQuality
SIO_000300: 1.699763e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.104e0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2140
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.294e0

DP
type: SiteQuality
SIO_000300: 1.699696e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1

MQ
type: SiteQuality
SIO_000300: 5.929e1

QD
type: SiteQuality
SIO_000300: 9.81e0

FS
type: SiteQuality
SIO_000300: 2.389e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2301
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8900
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 8
allele frequency: 4.847309743092584e-4
allele num: 16504
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.46e-1

DP
type: SiteQuality
SIO_000300: 1.699779e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.859e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.331e-1

FS
type: SiteQuality
SIO_000300: 2.265e0

QD
type: SiteQuality
SIO_000300: 1.205e1

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 943
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43628
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8899
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.285e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e0

VQSLOD
type: SiteQuality
SIO_000300: -5.354e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

DP
type: SiteQuality
SIO_000300: 1.699977e6

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43610
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.699968e6

VQSLOD
type: SiteQuality
SIO_000300: -1.804e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.81e-1

QD
type: SiteQuality
SIO_000300: 1.034e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

MQ
type: SiteQuality
SIO_000300: 5.744e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

MQRankSum
type: SiteQuality
SIO_000300: 2.49e0

FS
type: SiteQuality
SIO_000300: 6.069e0

GenotypeQuality
all individuals: 2291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 2.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 451
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.516e0

FS
type: SiteQuality
SIO_000300: 2.353e0

MQ
type: SiteQuality
SIO_000300: 5.862e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.68e-1

QD
type: SiteQuality
SIO_000300: 1.459e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.699941e6

VQSLOD
type: SiteQuality
SIO_000300: -1.044e0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2146
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43610
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.751e0

QD
type: SiteQuality
SIO_000300: 1.37e1

FS
type: SiteQuality
SIO_000300: 1.4641e1

MQRankSum
type: SiteQuality
SIO_000300: -5.71e-1

DP
type: SiteQuality
SIO_000300: 1.699942e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

MQ
type: SiteQuality
SIO_000300: 5.838e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

VQSLOD
type: SiteQuality
SIO_000300: -2.083e0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2290
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43603
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8896
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2143
bin: 7.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.09e0

VQSLOD
type: SiteQuality
SIO_000300: -1.707e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.96e-1

FS
type: SiteQuality
SIO_000300: 1.462e0

MQ
type: SiteQuality
SIO_000300: 5.843e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.42e1

DP
type: SiteQuality
SIO_000300: 1.699929e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.273e0

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

GenotypeQuality
all individuals: 2143
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8896
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 451
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1815
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 908
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 4.722e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.751e-1

DP
type: SiteQuality
SIO_000300: 1.699918e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

QD
type: SiteQuality
SIO_000300: 7.37e0

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

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

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

GenotypeQuality
all individuals: 1817
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43548
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.818402230573403e-4
allele num: 16498
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.17e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.83e0

DP
type: SiteQuality
SIO_000300: 1.700468e6

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.36e-1

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 932
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8854
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2449
bin: 9.75e1
variant carriers: 182

GenotypeQuality
all individuals: 2125
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 67
allele frequency: 1.004256849931051e-3
allele num: 66716
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.051175656984786e-4
allele num: 11568
num of homozygotes: 0

South Asian
type: Population
allele count: 106
allele frequency: 6.424242424242424e-3
allele num: 16500
num of homozygotes: 2

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

African
type: Population
allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.908e1

DP
type: SiteQuality
SIO_000300: 1.707407e6

MQRankSum
type: SiteQuality
SIO_000300: 5.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.57e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

FS
type: SiteQuality
SIO_000300: 5.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

QD
type: SiteQuality
SIO_000300: 1.364e1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
all individuals: 936
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 38
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8894
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 446
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1807
bin: 7.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQRankSum
type: SiteQuality
SIO_000300: -3.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.700379e6

MQ
type: SiteQuality
SIO_000300: 5.751e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.012e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

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

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2278
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2123
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8878
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43566
bin: 6.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.522e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

MQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

DP
type: SiteQuality
SIO_000300: 1.699898e6

QD
type: SiteQuality
SIO_000300: 1.5e1

MQ
type: SiteQuality
SIO_000300: 5.801e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e-1

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

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

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

GenotypeQuality
all individuals: 2279
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
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: 8652
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

FS
type: SiteQuality
SIO_000300: 9.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.064e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.699935e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

GenotypeQuality
all individuals: 8879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2118
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43585
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 448
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 445
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

DP
type: SiteQuality
SIO_000300: 1.699935e6

MQRankSum
type: SiteQuality
SIO_000300: 5.86e-1

QD
type: SiteQuality
SIO_000300: 1.064e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.24e-1

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

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2284
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1790
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8839
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 446
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.500075000750007e-5
allele num: 66666
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 5
allele frequency: 4.326756663205261e-4
allele num: 11556
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 1.303e1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.699254e6

FS
type: SiteQuality
SIO_000300: 1.152e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8823
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43262
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.092360180333861e-5
allele num: 16414
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.779010633379565e-4
allele num: 8652
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.698697e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 6.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.927e1

QD
type: SiteQuality
SIO_000300: 1.307e1

GenotypeQuality
all individuals: 921
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2093
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8798
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 9.75e1
variant carriers: 5

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.502070952638214e-5
allele num: 66636
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.119951040391677e-5
allele num: 16340
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.012e0

QD
type: SiteQuality
SIO_000300: 1.519e1

DP
type: SiteQuality
SIO_000300: 1.696215e6

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

GenotypeQuality
all individuals: 2096
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2272
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 444
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 366
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 443
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
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: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.477e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 5.876e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.946e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.599e1

MQRankSum
type: SiteQuality
SIO_000300: -2.048e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.486e0

VQSLOD
type: SiteQuality
SIO_000300: -3.496e0

DP
type: SiteQuality
SIO_000300: 1.694914e6

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1780
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42998
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2272
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 8789
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16242
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.884060757546626e-4
allele num: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66606
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.638e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

MQ
type: SiteQuality
SIO_000300: 5.813e1

DP
type: SiteQuality
SIO_000300: 1.693462e6

MQRankSum
type: SiteQuality
SIO_000300: 8.32e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

GenotypeQuality
all individuals: 2268
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 568
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8734
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 7.25e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.469812630117973e-4
allele num: 8646
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.19348445435402e-5
allele num: 16146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

QD
type: SiteQuality
SIO_000300: 1.313e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

FS
type: SiteQuality
SIO_000300: 4.245e0

DP
type: SiteQuality
SIO_000300: 1.691559e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
all individuals: 8688
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2066
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2265
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502990951994469e-5
allele num: 66534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16020
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: 11524
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.561e1

DP
type: SiteQuality
SIO_000300: 1.68779e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.67e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.045e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.498e-1

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2264
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 169
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503985561738607e-5
allele num: 66490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15912
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.684369e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

MQ
type: SiteQuality
SIO_000300: 5.831e1

VQSLOD
type: SiteQuality
SIO_000300: -2.121e0

FS
type: SiteQuality
SIO_000300: 1.034e0

QD
type: SiteQuality
SIO_000300: 3.314e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1721
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1411
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41687
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2260
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2015
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15660
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

FS
type: SiteQuality
SIO_000300: 1.145e0

MQ
type: SiteQuality
SIO_000300: 5.862e1

VQSLOD
type: SiteQuality
SIO_000300: -2.586e0

QD
type: SiteQuality
SIO_000300: 2.878e1

DP
type: SiteQuality
SIO_000300: 1.676213e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0