3-10320686-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320686
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320686
    reference: chr 3
allele count: 2
allele frequency: 1.64866870002473e-5
allele num: 121310
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*191A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.511A>G
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.2263A>G
  hgvsp: ENSP00000408736.2:p.Thr755Ala
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.526A>G
  hgvsp: ENSP00000389896.1:p.Thr176Ala
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1707A>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.2263A>G
  hgvsp: ENSP00000287652.4:p.Thr755Ala
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3413
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4631
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5710
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr755Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

3-10320692-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320692
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320692
    reference: chr 3
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.2269C>G
  hgvsp: ENSP00000408736.2:p.Arg757Gly
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.2269C>G
  hgvsp: ENSP00000287652.4:p.Arg757Gly
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.532C>G
  hgvsp: ENSP00000389896.1:p.Arg178Gly
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1713C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.517C>G
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*197C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3754
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20300
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg757Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

3-10320692-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320692
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320692
    reference: chr 3
allele count: 4
allele frequency: 3.297391763115376e-5
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.2269C>T
  hgvsp: ENSP00000287652.4:p.Arg757Cys
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.532C>T
  hgvsp: ENSP00000389896.1:p.Arg178Cys
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.517C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1713C>T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*197C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.2269C>T
  hgvsp: ENSP00000408736.2:p.Arg757Cys
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12096
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8112
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg757Cys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-10320693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320693
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320693
    reference: chr 3
allele count: 4
allele frequency: 3.297554863069035e-5
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.2270G>A
  hgvsp: ENSP00000287652.4:p.Arg757His
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*198G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.533G>A
  hgvsp: ENSP00000389896.1:p.Arg178His
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.2270G>A
  hgvsp: ENSP00000408736.2:p.Arg757His
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1714G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.518G>A
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13510
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3753
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg757His
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

3-10320693-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320693
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320693
    reference: chr 3
allele count: 2
allele frequency: 1.648777431534517e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1714G>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.2270G>T
  hgvsp: ENSP00000287652.4:p.Arg757Leu
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*198G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.2270G>T
  hgvsp: ENSP00000408736.2:p.Arg757Leu
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.518G>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.533G>T
  hgvsp: ENSP00000389896.1:p.Arg178Leu
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8113
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5705
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4632
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12099
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg757Leu
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

3-10320700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320700
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320700
    reference: chr 3
allele count: 20
allele frequency: 1.648777431534517e-4
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.2277C>T
  hgvsp: ENST00000448281.2:c.2277C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*205C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.525C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1721C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.540C>T
  hgvsp: ENST00000426850.1:c.540C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.2277C>T
  hgvsp: ENST00000287652.4:c.2277C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7641
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13503
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4380
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4629
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12113
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5706
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr759Tyr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

3-10320701-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320701
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320701
    reference: chr 3
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.541A>G
  hgvsp: ENSP00000389896.1:p.Ser181Gly
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.2278A>G
  hgvsp: ENSP00000287652.4:p.Ser760Gly
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*206A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.526A>G
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1722A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.2278A>G
  hgvsp: ENSP00000408736.2:p.Ser760Gly
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3413
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3749
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8117
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser760Gly
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

3-10320706-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320706
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320706
    reference: chr 3
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1727T>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.2283T>A
  hgvsp: ENST00000448281.2:c.2283T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.531T>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.546T>A
  hgvsp: ENST00000426850.1:c.546T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*211T>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.2283T>A
  hgvsp: ENST00000287652.4:c.2283T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20315
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5709
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4632
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Leu761Leu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

3-10320718-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320718
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320718
    reference: chr 3
allele count: 1
allele frequency: 8.251505899826718e-6
allele num: 121190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*9G>A
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7646
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4631
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3742
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5701
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20160
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: c.*9G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

3-10320719-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320719
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320719
    reference: chr 3
allele count: 1
allele frequency: 8.252459232851389e-6
allele num: 121176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+1G>T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+1G>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+1G>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+1G>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*10G>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*10G>T
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11306
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3414
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5704
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4632
  bin: 8.25e1
  variant carriers: 0
hgvs: c.*9+1G>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

3-10320720-TACAGTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320720
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320714
    reference: chr 3
allele count: 57
allele frequency: 4.70491126702435e-4
allele num: 121150
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+3_*223+8delACAGTC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+3_*1739+8delACAGTC
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+3_*9+8delACAGTC
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*12_*17delACAGTC
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*12_*17delACAGTC
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+3_543+8delACAGTC
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4375
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11266
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17485
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7639
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13459
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5700
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12143
  bin: 9.75e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4626
  bin: 8.25e1
  variant carriers: 0
hgvs: c.*9+3_*9+8delACAGTC
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: TACAGTC
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

3-10320722-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320722
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320722
    reference: chr 3
allele count: 8
allele frequency: 6.608730132505039e-5
allele num: 121052
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+4C>G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+4C>G
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*13C>G
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+4C>G
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+4C>G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*13C>G
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17441
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12098
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3734
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4628
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 2.25e1
  variant carriers: 0
hgvs: c.*9+4C>G
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-10320723-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320723
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320723
    reference: chr 3
allele count: 1
allele frequency: 8.265965712774223e-6
allele num: 120978
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+5A>C
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+5A>C
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*14A>C
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+5A>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*14A>C
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+5A>C
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12085
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7990
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
hgvs: c.*9+5A>C
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

3-10320726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320726
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320726
    reference: chr 3
allele count: 2
allele frequency: 1.652564780539397e-5
allele num: 121024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+8C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+8C>T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+8C>T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+8C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*17C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/28988
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7621
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4628
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5688
  bin: 7.75e1
  variant carriers: 0
hgvs: c.*9+8C>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP

3-10320729-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320729
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320729
    reference: chr 3
allele count: 8
allele frequency: 6.610149885148646e-5
allele num: 121026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+11C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+11C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*20C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+11C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+11C>T
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17274
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11103
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3408
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3725
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7957
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19538
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD

3-10320730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320730
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320730
    reference: chr 3
allele count: 9
allele frequency: 7.436787307882995e-5
allele num: 121020
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+12G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+12G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*21G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+12G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+12G>A
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4371
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3406
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3712
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

3-10320747-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320747
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320747
    reference: chr 3
allele count: 2
allele frequency: 1.655793621882969e-5
allele num: 120788
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+29G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+29G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+29G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*38G>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+29G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*38G>A
  variant of: http://identifiers.org/hgnc/28988
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4595
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5576
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
hgvs: c.*38G>A
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

3-10320747-GGTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320747
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320744
    reference: chr 3
allele count: 6
allele frequency: 4.967380865648906e-5
allele num: 120788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+32_*1739+34delCGT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*41_*43delCGT
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*38+3_*38+5delCGT
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+32_543+34delCGT
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+32_*223+34delCGT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+32_*9+34delCGT
  variant of: http://identifiers.org/hgnc/28988
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10399
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12806
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15734
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12103
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7272
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5576
  bin: 7.75e1
  variant carriers: 0
hgvs: c.*38+3_*38+5delCGT
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: GGTC
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/3-10320750-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320750
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320750
    reference: chr 3
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+32C>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+32C>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*41C>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+32C>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*38+3C>A
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+32C>A
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12098
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
hgvs: c.*38+3C>A
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

3-10320750-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10320750
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10320750
    reference: chr 3
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000389896
  ensembl transcript: ENST00000426850
  gene symbol: TATDN2
  hgvsc: ENST00000426850.1:c.*41C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000408736
  ensembl transcript: ENST00000448281
  gene symbol: TATDN2
  hgvsc: ENST00000448281.2:c.*38+3C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl transcript: ENST00000496355
  gene symbol: TATDN2
  hgvsc: ENST00000496355.1:n.543+32C>T
  variant of: http://identifiers.org/hgnc/28988
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*223+32C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*1739+32C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157014
  ensembl protein: ENSP00000287652
  ensembl transcript: ENST00000287652
  gene symbol: TATDN2
  hgvsc: ENST00000287652.4:c.*9+32C>T
  variant of: http://identifiers.org/hgnc/28988
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7488
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12098
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4596
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7165
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3405
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16371
  bin: 6.25e1
  variant carriers: 0
hgvs: c.*38+3C>T
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

3-10327478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327478
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327478
    reference: chr 3
allele count: 3
allele frequency: 2.480404802063697e-5
allele num: 120948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.41G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000399689
  ensembl transcript: ENST00000450534
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000450534.1:c.*2493G>A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000272410
  ensembl protein: ENSP00000402783
  ensembl transcript: ENST00000437082
  gene symbol: RP11-438J1.1
  hgvsc: ENST00000437082.1:c.*270G>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*50C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.612C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.41G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.526C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.41G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*81C>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

http://identifiers.org/exac.variant/3-10327488-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327488
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327488
    reference: chr 3
allele count: 1
allele frequency: 8.268289456277286e-6
allele num: 120944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*40G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*40G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.602G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.516G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.51C>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.51C>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.51C>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*71G>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD

3-10327490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327490
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327490
    reference: chr 3
allele count: 2
allele frequency: 1.652728655009421e-5
allele num: 121012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.53G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.514C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.53G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*38C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.53G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.600C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*69C>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

3-10327491-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327491
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327491
    reference: chr 3
allele count: 1
allele frequency: 8.266102367411717e-6
allele num: 120976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.54C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.599G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.54C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.54C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*68G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.513G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

3-10327501-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327501
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327501
    reference: chr 3
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.724G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*27G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.503G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*27G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.64C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.532G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.64C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*58G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.64C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.589G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

3-10327511-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327511
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327511
    reference: chr 3
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*17C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.522C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.74G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.714C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.74G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.74G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*48C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.579C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.493C>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5240
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

3-10327512-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327512
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327512
    reference: chr 3
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.521T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*16T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.75A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*16T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.713T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.578T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.492T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*47T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.75A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.75A>G
  variant of: http://identifiers.org/hgnc/33885
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD

3-10327514-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327514
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327514
    reference: chr 3
allele count: 2
allele frequency: 1.649430121892886e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*14C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.490C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.77G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.576C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.77G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.711C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*14C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.519C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.77G>A
  variant of: http://identifiers.org/hgnc/33885
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/3-10327517-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327517
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327517
    reference: chr 3
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.80C>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.708G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*11G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.516G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.80C>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.573G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*11G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.487G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.80C>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*42G>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

3-10327517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327517
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327517
    reference: chr 3
allele count: 3
allele frequency: 2.47390035129385e-5
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.80C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*11G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.80C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.516G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.80C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*11G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.487G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.573G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.708G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3103
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

3-10327522-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327522
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327522
    reference: chr 3
allele count: 7
allele frequency: 5.77072101037081e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.85C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.*6G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.568G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.85C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.*6G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.511G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.703G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.85C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.482G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

3-10327528-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327528
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327528
    reference: chr 3
allele count: 4
allele frequency: 3.297228679295053e-5
allele num: 121314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.476A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.91T>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.123A>C
  hgvsp: ENSP00000394923.2:p.Ter41TyrextTer2
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.276A>C
  hgvsp: ENSP00000405464.1:p.Ter92TyrextTer2
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.562A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.91T>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.505A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.91T>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.697A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*31A>C
  variant of: http://identifiers.org/hgnc/18129
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter92TyrextTer2
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

3-10327529-TAGAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327529
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327525
    reference: chr 3
allele count: 16
allele frequency: 1.318891471718021e-4
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.500_503delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.692_695delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.118_121delCTCT
  hgvsp: ENSP00000394923.2:p.Leu40Lys
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: frameshift_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.271_274delCTCT
  hgvsp: ENSP00000405464.1:p.Leu91Lys
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.97_100delAGAG
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.97_100delAGAG
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.97_100delAGAG
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.557_560delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.471_474delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*26_*29delCTCT
  variant of: http://identifiers.org/hgnc/18129
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu91Lys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: TAGAG
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

3-10327533-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327533
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327533
    reference: chr 3
allele count: 1
allele frequency: 8.24347940778844e-6
allele num: 121308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.118C>A
  hgvsp: ENSP00000394923.2:p.Leu40Ile
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.96G>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.471C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.557C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.96G>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.500C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.271C>A
  hgvsp: ENSP00000405464.1:p.Leu91Ile
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.96G>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*26C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.692C>A
  variant of: http://identifiers.org/hgnc/18129
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu91Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

3-10327542-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327542
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327542
    reference: chr 3
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.109C>G
  hgvsp: ENSP00000394923.2:p.Leu37Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.548C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+5G>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.491C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.262C>G
  hgvsp: ENSP00000405464.1:p.Leu88Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+5G>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+5G>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.683C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.462C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*17C>G
  variant of: http://identifiers.org/hgnc/18129
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu37Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-10327547-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327547
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327547
    reference: chr 3
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.457C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.257C>A
  hgvsp: ENSP00000405464.1:p.Ala86Asp
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.543C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.486C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.104C>A
  hgvsp: ENSP00000394923.2:p.Ala35Asp
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+10G>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*12C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+10G>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.678C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+10G>T
  variant of: http://identifiers.org/hgnc/33885
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10426
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala86Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

3-10327551-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327551
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327551
    reference: chr 3
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.453C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.100C>A
  hgvsp: ENSP00000394923.2:p.Gln34Lys
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.253C>A
  hgvsp: ENSP00000405464.1:p.Gln85Lys
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+14G>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+14G>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+14G>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.674C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.539C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.482C>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*8C>A
  variant of: http://identifiers.org/hgnc/18129
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln85Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD

3-10327556-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327556
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327556
    reference: chr 3
allele count: 22
allele frequency: 1.813117077914586e-4
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+19C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.477G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.448G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.534G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.95G>A
  hgvsp: ENSP00000394923.2:p.Arg32His
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.248G>A
  hgvsp: ENSP00000405464.1:p.Arg83His
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+19C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+19C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.669G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.*3G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10432
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg83His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

3-10327563-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327563
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327563
    reference: chr 3
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.441A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.350A>C
  hgvsp: ENSP00000335074.8:p.Lys117Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.527A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.241A>C
  hgvsp: ENSP00000405464.1:p.Ser81Arg
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.470A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+26T>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.197A>C
  hgvsp: ENSP00000403725.2:p.Lys66Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.350A>C
  hgvsp: ENSP00000389192.1:p.Lys117Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.350A>C
  hgvsp: ENSP00000414819.1:p.Lys117Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.314A>C
  hgvsp: ENSP00000416768.2:p.Lys105Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.347A>C
  hgvsp: ENSP00000415521.2:p.Lys116Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.662A>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.311A>C
  hgvsp: ENSP00000388145.2:p.Lys104Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+26T>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.88A>C
  hgvsp: ENSP00000394923.2:p.Ser30Arg
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.347A>C
  hgvsp: ENSP00000287656.7:p.Lys116Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+26T>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.350A>C
  hgvsp: ENSP00000391406.1:p.Lys117Thr
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.347A>C
  hgvsp: ENSP00000399922.1:p.Lys116Thr
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys117Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

3-10327567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327567
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327567
    reference: chr 3
allele count: 12
allele frequency: 9.890707680134513e-5
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+30C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.84G>A
  hgvsp: ENST00000446937.2:c.84G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.658G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.346G>A
  hgvsp: ENSP00000414819.1:p.Asp116Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.346G>A
  hgvsp: ENSP00000391406.1:p.Asp116Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.310G>A
  hgvsp: ENSP00000416768.2:p.Asp104Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.307G>A
  hgvsp: ENSP00000388145.2:p.Asp103Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.466G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.437G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.343G>A
  hgvsp: ENSP00000415521.2:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.343G>A
  hgvsp: ENSP00000399922.1:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.193G>A
  hgvsp: ENSP00000403725.2:p.Asp65Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.346G>A
  hgvsp: ENSP00000389192.1:p.Asp116Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+30C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+30C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.343G>A
  hgvsp: ENSP00000287656.7:p.Asp115Asn
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  clinical significance: not_provided
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.523G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  clinical significance: not_provided
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.346G>A
  hgvsp: ENSP00000335074.8:p.Asp116Asn
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp116Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

3-10327568-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327568
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327568
    reference: chr 3
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.342C>T
  hgvsp: ENST00000430179.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.436C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.522C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+31G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.309C>T
  hgvsp: ENST00000437422.2:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.83C>T
  hgvsp: ENSP00000394923.2:p.Pro28Leu
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.236C>T
  hgvsp: ENSP00000405464.1:p.Pro79Leu
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.345C>T
  hgvsp: ENST00000450603.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.345C>T
  hgvsp: ENST00000457360.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+31G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.345C>T
  hgvsp: ENST00000429122.1:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+31G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.345C>T
  hgvsp: ENST00000335542.8:c.345C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.342C>T
  hgvsp: ENST00000449554.2:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.306C>T
  hgvsp: ENST00000449238.2:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.465C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.192C>T
  hgvsp: ENST00000439975.2:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.342C>T
  hgvsp: ENST00000287656.7:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.657C>T
  variant of: http://identifiers.org/hgnc/18129
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro79Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP

3-10327569-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327569
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327569
    reference: chr 3
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.82C>T
  hgvsp: ENSP00000394923.2:p.Pro28Ser
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.344C>T
  hgvsp: ENSP00000335074.8:p.Ala115Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.344C>T
  hgvsp: ENSP00000391406.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.308C>T
  hgvsp: ENSP00000416768.2:p.Ala103Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.344C>T
  hgvsp: ENSP00000389192.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.341C>T
  hgvsp: ENSP00000287656.7:p.Ala114Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.435C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+32G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.341C>T
  hgvsp: ENSP00000399922.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.305C>T
  hgvsp: ENSP00000388145.2:p.Ala102Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.191C>T
  hgvsp: ENSP00000403725.2:p.Ala64Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.235C>T
  hgvsp: ENSP00000405464.1:p.Pro79Ser
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.656C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.344C>T
  hgvsp: ENSP00000414819.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+32G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+32G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.521C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.341C>T
  hgvsp: ENSP00000415521.2:p.Ala114Val
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.464C>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ala115Val
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: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

3-10327576-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327576
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327574
    reference: chr 3
allele count: 3
allele frequency: 2.472839974282464e-5
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73_74delAG
  hgvsp: ENSP00000394923.2:p.Arg25AlafsTer6
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332_333delAG
  hgvsp: ENSP00000415521.2:p.Glu111GlyfsTer?
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335_336delAG
  hgvsp: ENSP00000389192.1:p.Glu112GlyfsTer?
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226_227delAG
  hgvsp: ENSP00000405464.1:p.Arg76AlafsTer6
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+42_100+43delCT
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426_427delAG
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455_456delAG
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299_300delAG
  hgvsp: ENSP00000416768.2:p.Glu100GlyfsTer?
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296_297delAG
  hgvsp: ENSP00000388145.2:p.Glu99GlyfsTer?
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512_513delAG
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335_336delAG
  hgvsp: ENSP00000391406.1:p.Glu112GlyfsTer?
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332_333delAG
  hgvsp: ENSP00000399922.1:p.Glu111GlyfsTer?
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335_336delAG
  hgvsp: ENSP00000335074.8:p.Glu112GlyfsTer50
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332_333delAG
  hgvsp: ENSP00000287656.7:p.Glu111GlyfsTer?
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335_336delAG
  hgvsp: ENSP00000414819.1:p.Glu112GlyfsTer?
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+42_100+43delCT
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+42_100+43delCT
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647_648delAG
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu112GlyfsTer50
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: CCT
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

3-10327577-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327577
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327577
    reference: chr 3
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.336G>A
  hgvsp: ENST00000335542.8:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.183G>A
  hgvsp: ENST00000439975.2:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.456G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.300G>A
  hgvsp: ENST00000437422.2:c.300G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.336G>A
  hgvsp: ENST00000450603.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.513G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.297G>A
  hgvsp: ENST00000449238.2:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+40C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.427G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.227G>A
  hgvsp: ENSP00000405464.1:p.Arg76Lys
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.74G>A
  hgvsp: ENSP00000394923.2:p.Arg25Lys
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.333G>A
  hgvsp: ENST00000449554.2:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.336G>A
  hgvsp: ENST00000457360.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.333G>A
  hgvsp: ENST00000287656.7:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+40C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.333G>A
  hgvsp: ENST00000430179.1:c.333G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.648G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.336G>A
  hgvsp: ENST00000429122.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/18129
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg76Lys
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

3-10327588-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327588
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327588
    reference: chr 3
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+51A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+51A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+51A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-10T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-10T>C
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-10327594-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327594
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327594
    reference: chr 3
allele count: 13
allele frequency: 1.072094212340629e-4
allele num: 121258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+57T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+57T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+57T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-16A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-16A>G
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4691
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

3-10327603-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327603
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327603
    reference: chr 3
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+66A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+66A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+66A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-25T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-25T>C
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

3-10327604-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327604
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327604
    reference: chr 3
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+67A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+67A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-26T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+67A>G
  variant of: http://identifiers.org/hgnc/33885
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-10327614-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327614
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327614
    reference: chr 3
allele count: 3
allele frequency: 2.477496077297878e-5
allele num: 121090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+77C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+77C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+77C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-36G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-36G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4031
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

3-10327615-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327615
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327615
    reference: chr 3
allele count: 1
allele frequency: 8.255729476256522e-6
allele num: 121128
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+78A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+78A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+78A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-37T>C
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

3-10327616-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327616
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327616
    reference: chr 3
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+79C>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+79C>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+79C>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-38G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-38G>C
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-10327618-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327618
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327618
    reference: chr 3
allele count: 31
allele frequency: 2.56012156448203e-4
allele num: 121088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+81G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+81G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+81G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-40C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-40C>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

3-10327625-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327625
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327625
    reference: chr 3
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+88T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+88T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+88T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-47A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-47A>G
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

3-10327627-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10327627
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10327627
    reference: chr 3
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.332-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.335-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.335-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.335-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.100+90G>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.647-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.455-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+90G>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.332-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.335-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.296-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.299-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.426-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.512-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.100+90G>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.182-49C>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.332-49C>G
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

3-10328338-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328338
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328338
    reference: chr 3
allele count: 2
allele frequency: 1.772798184654659e-5
allele num: 112816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-760C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-760G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-760G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-760C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+801C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+50G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+50G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17107
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

3-10328342-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328342
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328342
    reference: chr 3
allele count: 1
allele frequency: 8.836888708223609e-6
allele num: 113162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-756T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-764A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+805T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-756T>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+46A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-764A>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+46A>G
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2218
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-10328343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328343
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328343
    reference: chr 3
allele count: 1
allele frequency: 8.837513477208053e-6
allele num: 113154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-755G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-765C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+806G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-755G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+45C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-765C>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

3-10328350-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328350
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328350
    reference: chr 3
allele count: 1
allele frequency: 8.802042073761113e-6
allele num: 113610
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-772G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-748C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-748C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+813C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-772G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+38G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+38G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9025
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-10328351-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328351
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328351
    reference: chr 3
allele count: 2
allele frequency: 1.755802928679285e-5
allele num: 113908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-747A>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-773T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+814A>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-773T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-747A>C
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+37T>G
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+37T>G
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11414
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

3-10328351-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328351
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328351
    reference: chr 3
allele count: 2
allele frequency: 1.755802928679285e-5
allele num: 113908
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-747A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-747A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+814A>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-773T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-773T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+37T>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+37T>C
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

3-10328359-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328359
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328359
    reference: chr 3
allele count: 17
allele frequency: 1.485390745141898e-4
allele num: 114448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-781G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+822C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-739C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-781G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-739C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+29G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+29G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

3-10328360-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328360
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328360
    reference: chr 3
allele count: 1
allele frequency: 8.707615680674318e-6
allele num: 114842
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-738G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-782C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-782C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+823G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+28C>T
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-738G>A
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+28C>T
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum

3-10328367-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328367
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328367
    reference: chr 3
allele count: 1
allele frequency: 8.616975441619991e-6
allele num: 116050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-731C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-789G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-789G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+830C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+21G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-731C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+21G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

3-10328368-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328368
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328368
    reference: chr 3
allele count: 2
allele frequency: 1.720874204095681e-5
allele num: 116220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000476283
  gene symbol: GHRL
  hgvsc: ENST00000476283.1:n.646+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000416768
  ensembl transcript: ENST00000437422
  gene symbol: GHRL
  hgvsc: ENST00000437422.2:c.298+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000491589
  gene symbol: GHRL
  hgvsc: ENST00000491589.1:n.425+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-730C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000391406
  ensembl transcript: ENST00000457360
  gene symbol: GHRL
  hgvsc: ENST00000457360.1:c.334+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-790G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000439539
  gene symbol: GHRLOS
  hgvsc: ENST00000439539.3:n.101-730C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605105
  gene symbol: GHRLOS
  hgvsc: ENST00000605105.1:n.100+831C>T
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000403725
  ensembl transcript: ENST00000439975
  gene symbol: GHRL
  hgvsc: ENST00000439975.2:c.181+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+20G>A
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-790G>A
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

3-10328385-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10328385
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 10328385
    reference: chr 3
allele count: 1
allele frequency: 8.410994852471151e-6
allele num: 118892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000481287
  gene symbol: GHRL
  hgvsc: ENST00000481287.1:n.511+3G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000388145
  ensembl transcript: ENST00000449238
  gene symbol: GHRL
  hgvsc: ENST00000449238.2:c.295+3G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000335074
  ensembl transcript: ENST00000335542
  gene symbol: GHRL
  hgvsc: ENST00000335542.8:c.334+3G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000399922
  ensembl transcript: ENST00000430179
  gene symbol: GHRL
  hgvsc: ENST00000430179.1:c.331+3G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000240288
  ensembl transcript: ENST00000605014
  gene symbol: GHRLOS
  hgvsc: ENST00000605014.1:n.101-713C>G
  variant of: http://identifiers.org/hgnc/33885
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000405464
  ensembl transcript: ENST00000422159
  gene symbol: GHRL
  hgvsc: ENST00000422159.1:c.226-807G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000287656
  ensembl transcript: ENST00000287656
  gene symbol: GHRL
  hgvsc: ENST00000287656.7:c.331+3G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000394923
  ensembl transcript: ENST00000446937
  gene symbol: GHRL
  hgvsc: ENST00000446937.2:c.73-807G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000389192
  ensembl transcript: ENST00000450603
  gene symbol: GHRL
  hgvsc: ENST00000450603.1:c.334+3G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000415521
  ensembl transcript: ENST00000449554
  gene symbol: GHRL
  hgvsc: ENST00000449554.2:c.331+3G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl transcript: ENST00000475759
  gene symbol: GHRL
  hgvsc: ENST00000475759.1:n.454+3G>C
  variant of: http://identifiers.org/hgnc/18129
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000157017
  ensembl protein: ENSP00000414819
  ensembl transcript: ENST00000429122
  gene symbol: GHRL
  hgvsc: ENST00000429122.1:c.334+3G>C
  variant of: http://identifiers.org/hgnc/18129
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
hgvs: c.334+3G>C
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 8112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3756
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20304
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12094
bin: 9.75e1
variant carriers: 2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

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

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

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: 2
allele frequency: 2.999580058791769e-5
allele num: 66676
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: -2.896e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.51e-1

QD
type: SiteQuality
SIO_000300: 8.59e0

FS
type: SiteQuality
SIO_000300: 2.653e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 1.967096e6

GenotypeQuality
all individuals: 8112
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12096
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5707
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4632
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: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
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: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
type: SiteQuality
SIO_000300: 1.96724e6

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

FS
type: SiteQuality
SIO_000300: 4.916e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.238e1

GenotypeQuality
all individuals: 5707
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4632
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2367
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3754
bin: 7.25e1
variant carriers: 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: 10400
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.998980173370527e-5
allele num: 66678
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

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.96724e6

FS
type: SiteQuality
SIO_000300: 4.916e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.238e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -9.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.62e-1

GenotypeQuality
all individuals: 20301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4632
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12099
bin: 9.75e1
variant carriers: 4

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.311604253351826e-4
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: 1
allele frequency: 6.067961165048543e-5
allele num: 16480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

DP
type: SiteQuality
SIO_000300: 1.967269e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.44e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.196e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3753
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2365
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20301
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
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: 11572
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.196e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

FS
type: SiteQuality
SIO_000300: 5.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.19e-1

DP
type: SiteQuality
SIO_000300: 1.967269e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

GenotypeQuality
all individuals: 20318
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8113
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3747
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3414
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
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: 17
allele frequency: 1.031553398058253e-3
allele num: 16480
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 3
allele frequency: 3.468208092485549e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.089e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.311e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.9674e6

GenotypeQuality
all individuals: 2362
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20325
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5708
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
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: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.175e1

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.966843e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 4.023e0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
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: 10396
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e0

QD
type: SiteQuality
SIO_000300: 1.025e1

DP
type: SiteQuality
SIO_000300: 1.966648e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 2363
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

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

South Asian
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allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.718e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.55e-1

DP
type: SiteQuality
SIO_000300: 1.964385e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

FS
type: SiteQuality
SIO_000300: 6.6e-1

MQ
type: SiteQuality
SIO_000300: 5.82e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
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: 16434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.229e0

QD
type: SiteQuality
SIO_000300: 8.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.504e0

VQSLOD
type: SiteQuality
SIO_000300: -5.944e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

DP
type: SiteQuality
SIO_000300: 1.963853e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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: 1.500330072615976e-5
allele num: 66652
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: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 53
allele frequency: 5.130687318489835e-3
allele num: 10330
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16426
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.8e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

FS
type: SiteQuality
SIO_000300: 1.905e0

DP
type: SiteQuality
SIO_000300: 1.964408e6

MQRankSum
type: SiteQuality
SIO_000300: -4.993e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.58e-1

QD
type: SiteQuality
SIO_000300: 6.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.193e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 2362
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.873294346978557e-4
allele num: 16416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.629999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.961382e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.03e-1

QD
type: SiteQuality
SIO_000300: 1.148e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.11e-1

FS
type: SiteQuality
SIO_000300: 5.679999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.36e0

GenotypeQuality
all individuals: 5689
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 2362
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 173
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 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: 10220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66632
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.09979260705136e-5
allele num: 16394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
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: 11570
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.77e0

VQSLOD
type: SiteQuality
SIO_000300: -6.477000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.87e-1

DP
type: SiteQuality
SIO_000300: 1.956475e6

FS
type: SiteQuality
SIO_000300: 5.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 442
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variant carriers: 0

GenotypeQuality
all individuals: 72
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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: 2
allele frequency: 3.00147072065312e-5
allele num: 66634
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-1

MQ
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.872e0

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.958524e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

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

South Asian
type: Population
allele count: 7
allele frequency: 4.273504273504274e-4
allele num: 16380
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: 9.714396735962697e-5
allele num: 10294
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
SIO_000300: 1.955805e6

QD
type: SiteQuality
SIO_000300: 1.249e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.56e-1

FS
type: SiteQuality
SIO_000300: 5.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.78e0

GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12101
bin: 9.75e1
variant carriers: 9

GenotypeQuality
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bin: 8.25e1
variant carriers: 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

African
type: Population
allele count: 4
allele frequency: 3.88651379712398e-4
allele num: 10292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.505253677574302e-5
allele num: 66620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

FS
type: SiteQuality
SIO_000300: 1.115e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

QD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 12103
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 908
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GenotypeQuality
all individuals: 17245
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66568
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.957713390759593e-4
allele num: 10216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: -3.86e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.536e0

DP
type: SiteQuality
SIO_000300: 1.922356e6

FS
type: SiteQuality
SIO_000300: 2.51e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.612e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.75e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 933
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GenotypeQuality
all individuals: 17245
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GenotypeQuality
all individuals: 406
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GenotypeQuality
all individuals: 2351
bin: 8.75e1
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GenotypeQuality
all individuals: 3575
bin: 7.25e1
variant carriers: 0

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

African
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.729804532087874e-4
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.008893161879582e-5
allele num: 66568
num of homozygotes: 0

East Asian
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Other
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MQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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FS
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BaseQRankSum
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MQ
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QD
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InbreedingCoeff
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SIO_000300: 2.4e-3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

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

Latino
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South Asian
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Other
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East Asian
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European (Non-Finnish)
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allele frequency: 1.503307276007216e-5
allele num: 66520
num of homozygotes: 0

African
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MQ
type: SiteQuality
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QD
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InbreedingCoeff
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SIO_000300: 2.5e-3

BaseQRankSum
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VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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SIO_000300: 6.3e-2

ReadPosRankSum
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DP
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SIO_000300: 1.914791e6

GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

South Asian
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Latino
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allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

East Asian
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allele count: 0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
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ReadPosRankSum
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SIO_000300: 9.370000000000001e-1

DP
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SIO_000300: 4.304022e6

MQRankSum
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SIO_000300: -5.42e-1

VQSLOD
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ClippingRankSum
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SIO_000300: -2.06e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 4.323e0

QD
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SIO_000300: 1.407e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
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allele num: 8654
num of homozygotes: 0

South Asian
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allele frequency: 6.154603643525357e-5
allele num: 16248
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Latino
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FS
type: SiteQuality
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

European (Finnish)
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Other
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South Asian
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African
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European (Non-Finnish)
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East Asian
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BaseQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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Other
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African
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European (Non-Finnish)
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allele num: 66554
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Latino
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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MQRankSum
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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InbreedingCoeff
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DP
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MQ
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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FS
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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MQ
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GenotypeQuality
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African
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South Asian
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Latino
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FS
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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East Asian
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South Asian
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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South Asian
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MQRankSum
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InbreedingCoeff
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QD
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FS
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BaseQRankSum
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MQ
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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African
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South Asian
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DP
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MQ
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QD
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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South Asian
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East Asian
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European (Non-Finnish)
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VQSLOD
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FS
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MQRankSum
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European (Finnish)
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African
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South Asian
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GenotypeQuality
all individuals: 346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.75e1
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: 16498
num of homozygotes: 0

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

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: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.79e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

DP
type: SiteQuality
SIO_000300: 4.327073e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 3.685e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.6e-2

GenotypeDepth
all individuals: 5248
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1162
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5443
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4694
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4032
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3546
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3152
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1908
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4415
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 938
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variant carriers: 0

GenotypeDepth
all individuals: 2920
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3090
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5241
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 834
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4342
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 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: 8654
num of homozygotes: 0

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 4.327147e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.223e0

VQSLOD
type: SiteQuality
SIO_000300: 2.53e-1

GenotypeDepth
all individuals: 5444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4415
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3090
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5241
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1161
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2089
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1915
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2920
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5248
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3546
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10425
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4694
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4032
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2348
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53101
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 351
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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: 11578
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: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.881e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.027e0

FS
type: SiteQuality
SIO_000300: 8.129999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

VQSLOD
type: SiteQuality
SIO_000300: -8.656e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.14e0

DP
type: SiteQuality
SIO_000300: 4.327393e6

QD
type: SiteQuality
SIO_000300: 1.114e1

GenotypeDepth
all individuals: 5444
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5247
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2089
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4693
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3135
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1923
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5241
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4033
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 945
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2348
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2919
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1161
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3088
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4334
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 441
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53104
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.549643049973004e-4
allele num: 66676
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817741153659719e-4
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

FS
type: SiteQuality
SIO_000300: 5.29e-1

DP
type: SiteQuality
SIO_000300: 4.328603e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.7e-1

QD
type: SiteQuality
SIO_000300: 1.03e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

GenotypeDepth
all individuals: 5247
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1162
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2348
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3119
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 941
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10424
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 2088
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3545
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4692
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5445
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3089
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4034
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1937
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2917
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5244
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4415
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 350
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4338
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53098
bin: 9.75e1
variant carriers: 2

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: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 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: 16506
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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
SIO_000300: 4.327047e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 4.328e0

VQSLOD
type: SiteQuality
SIO_000300: -6.298e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e0

Annotation
canonical: false
clinical significance: not_provided
consequence: synonymous_variant
ensembl gene: ENSG00000157017
ensembl protein: ENSP00000405464
ensembl transcript: ENST00000422159
gene symbol: GHRL
hgvsc: ENST00000422159.1:c.237G>A
hgvsp: ENST00000422159.1:c.237G>A(p.%3D)
variant of: http://identifiers.org/hgnc/18129

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 42
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1160
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2917
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2088
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3089
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5244
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4415
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1943
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10432
bin: 9.75e1
variant carriers: 12

GenotypeDepth
all individuals: 2347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4691
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 944
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3544
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5246
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3098
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5443
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4033
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53099
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4313
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
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: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.77336327517706e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
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: 908
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

DP
type: SiteQuality
SIO_000300: 4.327582e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.219e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.65e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeDepth
all individuals: 2089
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3546
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3099
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10422
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5247
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1942
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4034
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4417
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5246
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2916
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1160
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4692
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 942
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3090
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 529
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4320
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53099
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 834
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 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: 11578
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

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: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500015000150001e-5
allele num: 66666
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.811e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.629999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

QD
type: SiteQuality
SIO_000300: 1.479e1

VQSLOD
type: SiteQuality
SIO_000300: -1.231e0

MQ
type: SiteQuality
SIO_000300: 5.86e1

DP
type: SiteQuality
SIO_000300: 4.326814e6

GenotypeDepth
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5246
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5247
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1942
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4033
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 944
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 44
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3095
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2917
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5444
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4692
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2088
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4417
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3546
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3090
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1161
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10422
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
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: 4317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 349
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53099
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 833
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
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: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

FS
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 4.326757e6

MQRankSum
type: SiteQuality
SIO_000300: 4.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.487e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.226e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.215e0

Annotation
canonical: false
consequence: frameshift_variant
consequence: splice_region_variant
ensembl gene: ENSG00000157017
ensembl protein: ENSP00000403725
ensembl transcript: ENST00000439975
gene symbol: GHRL
hgvsc: ENST00000439975.2:c.182_183delAG
hgvsp: ENSP00000403725.2:p.Glu61GlyfsTer?
variant of: http://identifiers.org/hgnc/18129

GenotypeDepth
all individuals: 5443
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5246
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10422
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 940
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2918
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4033
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3546
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1161
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4692
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1954
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2088
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3091
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4418
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5246
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3061
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4290
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53101
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

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

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: 3
allele frequency: 1.818843215714805e-4
allele num: 16494
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

DP
type: SiteQuality
SIO_000300: 4.326578e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.991e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.226e0

MQRankSum
type: SiteQuality
SIO_000300: -9.8e-2

QD
type: SiteQuality
SIO_000300: 1.541e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000240288
ensembl transcript: ENST00000605105
gene symbol: GHRLOS
hgvsc: ENST00000605105.1:n.100+40C>T
variant of: http://identifiers.org/hgnc/33885

GenotypeDepth
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2917
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4418
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1160
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3546
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2347
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10422
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2088
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5443
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5246
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4033
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 941
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4692
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5246
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1957
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3053
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3090
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 529
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53098
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 826
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4284
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 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: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.212e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.446e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

DP
type: SiteQuality
SIO_000300: 4.326464e6

FS
type: SiteQuality
SIO_000300: 1.2135e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.592e0

QD
type: SiteQuality
SIO_000300: 1.13e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeDepth
all individuals: 3546
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4033
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2927
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 117
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4691
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1162
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1947
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4418
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2087
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 0
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 61
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2348
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10422
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3090
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5246
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2917
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4167
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 817
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53098
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

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

InbreedingCoeff
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MQ
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ReadPosRankSum
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SIO_000300: 9.59e-1

FS
type: SiteQuality
SIO_000300: 2.4179e1

DP
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MQRankSum
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SIO_000300: 2.21e-1

VQSLOD
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QD
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SIO_000300: 1.503e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-1

BaseQRankSum
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SIO_000300: 6.81e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

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

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

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

African
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Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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FS
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SIO_000300: 1.1509e1

MQ
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BaseQRankSum
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MQRankSum
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DP
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: 1.2e-3

ReadPosRankSum
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SIO_000300: -7.0e-3

ClippingRankSum
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SIO_000300: -2.28e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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variant carriers: 4

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

Latino
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allele count: 24
allele frequency: 2.074688796680498e-3
allele num: 11568
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

Other
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allele num: 906
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.111722283339445e-5
allele num: 16362
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.509762691498949e-5
allele num: 66580
num of homozygotes: 0

DP
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SIO_000300: 4.308691e6

InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -3.589e0

VQSLOD
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SIO_000300: 3.35e0

MQ
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SIO_000300: 5.975e1

QD
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GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 3.098e0

ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: 3.4e-3

QD
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SIO_000300: 1.704e1

DP
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SIO_000300: 4.305544e6

GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

FS
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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MQ
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QD
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.054231717337716e-4
allele num: 9736
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10610
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6014
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62446
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: -1.8e-3

MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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VQSLOD
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DP
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ReadPosRankSum
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QD
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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QD
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ClippingRankSum
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MQRankSum
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MQ
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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South Asian
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East Asian
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VQSLOD
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FS
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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South Asian
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East Asian
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European (Finnish)
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FS
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQ
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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BaseQRankSum
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FS
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MQ
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QD
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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FS
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QD
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VQSLOD
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MQ
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DP
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4197
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1439
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3597
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3922
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1755
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 346
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32187
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 639
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4075
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.49102377486657e-4
allele num: 8244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.482268158543523e-5
allele num: 63276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10844
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9844
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.614720878546215e-4
allele num: 15298
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

QD
type: SiteQuality
SIO_000300: 1.222e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 3.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

DP
type: SiteQuality
SIO_000300: 1.314262e6

GenotypeDepth
all individuals: 108
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7939
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29457
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 55
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 145
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2668
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3045
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 69
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 506
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11236
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4057
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1241
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 714
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34455
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3532
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 657
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4319
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1170
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3063
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1742
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.575398575839688e-5
allele num: 63476
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -6.902e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 8.6e0

DP
type: SiteQuality
SIO_000300: 1.331643e6

FS
type: SiteQuality
SIO_000300: 6.575e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

GenotypeDepth
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2130
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2830
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12318
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 32
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5084
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33263
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 510
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1282
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3308
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 683
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38868
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558943659776136e-5
allele num: 64146
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.451e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 2.208e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.383148e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

GenotypeDepth
all individuals: 55
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 144
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 43
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 509
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2888
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2060
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 33266
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 69
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 308
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12613
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4866
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 933
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 52
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 676
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1749
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 890
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3228
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4725
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.415191172696946e-5
allele num: 15588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64224
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11040
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.004419445560466e-4
allele num: 9956
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.358e0

QD
type: SiteQuality
SIO_000300: 1.29e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

DP
type: SiteQuality
SIO_000300: 1.389026e6