2-33614218-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614218
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614218
    reference: chr 2
allele count: 7
allele frequency: 5.783881149505065e-5
allele num: 121026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-33G>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-33G>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-33G>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-33G>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-33G>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-33G>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-33G>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-33G>C
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4583
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

2-33614223-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614223
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614223
    reference: chr 2
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-28G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-28G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-28G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-28G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-28G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-28G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-28G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-28G>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4776
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

2-33614224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614224
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614224
    reference: chr 2
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-27G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-27G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-27G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-27G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-27G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-27G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-27G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-27G>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1300
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4766
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

2-33614229-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614229
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614229
    reference: chr 2
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-22A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-22A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-22A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-22A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-22A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-22A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-22A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-22A>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3293
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6983
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5111
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

2-33614234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614234
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614234
    reference: chr 2
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-17G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-17G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-17G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-17G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-17G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-17G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-17G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-17G>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6982
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5295
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

2-33614237-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614237
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614237
    reference: chr 2
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-14T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-14T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-14T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-14T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-14T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-14T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-14T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-14T>C
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6982
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1305
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-33614239-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614239
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614239
    reference: chr 2
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-12T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-12T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-12T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-12T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-12T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-12T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-12T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-12T>C
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5395
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum

2-33614241-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614241
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614241
    reference: chr 2
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-10T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-10T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-10T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-10T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-10T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-10T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-10T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-10T>C
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48290
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

2-33614242-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614242
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614242
    reference: chr 2
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-9A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-9A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-9A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-9A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-9A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-9A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-9A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-9A>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5429
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-33614245-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614245
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614245
    reference: chr 2
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3569-6C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4712-6C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3575-6C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3737-6C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1406-6C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3608-6C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4715-6C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3734-6C>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5477
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 8.25e1
  variant carriers: 0
hgvs: c.4712-6C>A
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

2-33614264-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614264
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614264
    reference: chr 2
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3621G>A
  hgvsp: ENST00000418533.2:c.3621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4725G>A
  hgvsp: ENST00000404816.2:c.4725G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3582G>A
  hgvsp: ENST00000402934.1:c.3582G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3588G>A
  hgvsp: ENST00000404525.1:c.3588G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3747G>A
  hgvsp: ENST00000407925.1:c.3747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3750G>A
  hgvsp: ENST00000390003.4:c.3750G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1419G>A
  hgvsp: ENST00000272273.5:c.1419G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4728G>A
  hgvsp: ENST00000354476.3:c.4728G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6979
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 781
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln1575Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-33614276-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614276
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614276
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3633C>A
  hgvsp: ENST00000418533.2:c.3633C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1431C>A
  hgvsp: ENST00000272273.5:c.1431C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3762C>A
  hgvsp: ENST00000390003.4:c.3762C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4737C>A
  hgvsp: ENST00000404816.2:c.4737C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3600C>A
  hgvsp: ENST00000404525.1:c.3600C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3594C>A
  hgvsp: ENST00000402934.1:c.3594C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3759C>A
  hgvsp: ENST00000407925.1:c.3759C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4740C>A
  hgvsp: ENST00000354476.3:c.4740C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3455
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile1579Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

2-33614277-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614277
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614277
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1432C>T
  hgvsp: ENSP00000272273.5:p.Pro478Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3763C>T
  hgvsp: ENSP00000374653.4:p.Pro1255Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3634C>T
  hgvsp: ENSP00000393057.2:p.Pro1212Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3601C>T
  hgvsp: ENSP00000385359.1:p.Pro1201Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3595C>T
  hgvsp: ENSP00000384373.1:p.Pro1199Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4741C>T
  hgvsp: ENSP00000346467.3:p.Pro1581Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3760C>T
  hgvsp: ENSP00000384091.1:p.Pro1254Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4738C>T
  hgvsp: ENSP00000386043.2:p.Pro1580Ser
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5064
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1310
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48291
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro1580Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

2-33614278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614278
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614278
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4742C>T
  hgvsp: ENSP00000346467.3:p.Pro1581Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3602C>T
  hgvsp: ENSP00000385359.1:p.Pro1201Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3596C>T
  hgvsp: ENSP00000384373.1:p.Pro1199Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4739C>T
  hgvsp: ENSP00000386043.2:p.Pro1580Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1433C>T
  hgvsp: ENSP00000272273.5:p.Pro478Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3764C>T
  hgvsp: ENSP00000374653.4:p.Pro1255Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3635C>T
  hgvsp: ENSP00000393057.2:p.Pro1212Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3761C>T
  hgvsp: ENSP00000384091.1:p.Pro1254Leu
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro1580Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-33614279-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614279
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614279
    reference: chr 2
allele count: 12
allele frequency: 9.884841595413434e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3765C>T
  hgvsp: ENST00000390003.4:c.3765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4740C>T
  hgvsp: ENST00000404816.2:c.4740C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3636C>T
  hgvsp: ENST00000418533.2:c.3636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3597C>T
  hgvsp: ENST00000402934.1:c.3597C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4743C>T
  hgvsp: ENST00000354476.3:c.4743C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3603C>T
  hgvsp: ENST00000404525.1:c.3603C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3762C>T
  hgvsp: ENST00000407925.1:c.3762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1434C>T
  hgvsp: ENST00000272273.5:c.1434C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 9.75e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro1580Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

2-33614280-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614280
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614280
    reference: chr 2
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3598G>C
  hgvsp: ENSP00000384373.1:p.Val1200Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4741G>C
  hgvsp: ENSP00000386043.2:p.Val1581Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3637G>C
  hgvsp: ENSP00000393057.2:p.Val1213Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3604G>C
  hgvsp: ENSP00000385359.1:p.Val1202Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4744G>C
  hgvsp: ENSP00000346467.3:p.Val1582Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1435G>C
  hgvsp: ENSP00000272273.5:p.Val479Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3763G>C
  hgvsp: ENSP00000384091.1:p.Val1255Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3766G>C
  hgvsp: ENSP00000374653.4:p.Val1256Leu
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5627
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 777
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val1581Leu
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

2-33614281-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614281
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614281
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1436T>C
  hgvsp: ENSP00000272273.5:p.Val479Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3599T>C
  hgvsp: ENSP00000384373.1:p.Val1200Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3764T>C
  hgvsp: ENSP00000384091.1:p.Val1255Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3767T>C
  hgvsp: ENSP00000374653.4:p.Val1256Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4742T>C
  hgvsp: ENSP00000386043.2:p.Val1581Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3638T>C
  hgvsp: ENSP00000393057.2:p.Val1213Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3605T>C
  hgvsp: ENSP00000385359.1:p.Val1202Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4745T>C
  hgvsp: ENSP00000346467.3:p.Val1582Ala
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val1581Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

2-33614284-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614284
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614284
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3770C>G
  hgvsp: ENSP00000374653.4:p.Thr1257Arg
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3767C>G
  hgvsp: ENSP00000384091.1:p.Thr1256Arg
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3602C>G
  hgvsp: ENSP00000384373.1:p.Thr1201Arg
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3608C>G
  hgvsp: ENSP00000385359.1:p.Thr1203Arg
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3641C>G
  hgvsp: ENSP00000393057.2:p.Thr1214Arg
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4748C>G
  hgvsp: ENSP00000346467.3:p.Thr1583Arg
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1439C>G
  hgvsp: ENSP00000272273.5:p.Thr480Arg
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4745C>G
  hgvsp: ENSP00000386043.2:p.Thr1582Arg
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6967
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48288
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr1582Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

2-33614284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614284
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614284
    reference: chr 2
allele count: 10
allele frequency: 8.237232289950576e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3767C>T
  hgvsp: ENSP00000384091.1:p.Thr1256Met
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3770C>T
  hgvsp: ENSP00000374653.4:p.Thr1257Met
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4748C>T
  hgvsp: ENSP00000346467.3:p.Thr1583Met
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3608C>T
  hgvsp: ENSP00000385359.1:p.Thr1203Met
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1439C>T
  hgvsp: ENSP00000272273.5:p.Thr480Met
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3641C>T
  hgvsp: ENSP00000393057.2:p.Thr1214Met
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4745C>T
  hgvsp: ENSP00000386043.2:p.Thr1582Met
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3602C>T
  hgvsp: ENSP00000384373.1:p.Thr1201Met
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6967
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48288
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5598
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr1582Met
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

2-33614285-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614285
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614285
    reference: chr 2
allele count: 4
allele frequency: 3.29489291598023e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3603G>A
  hgvsp: ENST00000402934.1:c.3603G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3642G>A
  hgvsp: ENST00000418533.2:c.3642G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4746G>A
  hgvsp: ENST00000404816.2:c.4746G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1440G>A
  hgvsp: ENST00000272273.5:c.1440G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3768G>A
  hgvsp: ENST00000407925.1:c.3768G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4749G>A
  hgvsp: ENST00000354476.3:c.4749G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3609G>A
  hgvsp: ENST00000404525.1:c.3609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3771G>A
  hgvsp: ENST00000390003.4:c.3771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6963
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr1582Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD

2-33614290-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614290
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614290
    reference: chr 2
allele count: 3
allele frequency: 2.471210398853358e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3608G>A
  hgvsp: ENSP00000384373.1:p.Arg1203His
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3776G>A
  hgvsp: ENSP00000374653.4:p.Arg1259His
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3773G>A
  hgvsp: ENSP00000384091.1:p.Arg1258His
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3647G>A
  hgvsp: ENSP00000393057.2:p.Arg1216His
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3614G>A
  hgvsp: ENSP00000385359.1:p.Arg1205His
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1445G>A
  hgvsp: ENSP00000272273.5:p.Arg482His
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4751G>A
  hgvsp: ENSP00000386043.2:p.Arg1584His
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4754G>A
  hgvsp: ENSP00000346467.3:p.Arg1585His
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg1584His
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

2-33614291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614291
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614291
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3648C>T
  hgvsp: ENST00000418533.2:c.3648C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4755C>T
  hgvsp: ENST00000354476.3:c.4755C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3609C>T
  hgvsp: ENST00000402934.1:c.3609C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3774C>T
  hgvsp: ENST00000407925.1:c.3774C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1446C>T
  hgvsp: ENST00000272273.5:c.1446C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3777C>T
  hgvsp: ENST00000390003.4:c.3777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4752C>T
  hgvsp: ENST00000404816.2:c.4752C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3615C>T
  hgvsp: ENST00000404525.1:c.3615C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6960
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg1584Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

2-33614292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614292
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614292
    reference: chr 2
allele count: 6
allele frequency: 4.942257952916756e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3778C>T
  hgvsp: ENSP00000374653.4:p.Arg1260Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3775C>T
  hgvsp: ENSP00000384091.1:p.Arg1259Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1447C>T
  hgvsp: ENSP00000272273.5:p.Arg483Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4756C>T
  hgvsp: ENSP00000346467.3:p.Arg1586Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3610C>T
  hgvsp: ENSP00000384373.1:p.Arg1204Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3616C>T
  hgvsp: ENSP00000385359.1:p.Arg1206Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4753C>T
  hgvsp: ENSP00000386043.2:p.Arg1585Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3649C>T
  hgvsp: ENSP00000393057.2:p.Arg1217Trp
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2203
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6961
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1304
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg1585Trp
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

2-33614293-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614293
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614293
    reference: chr 2
allele count: 2
allele frequency: 1.647419317638919e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3779G>T
  hgvsp: ENSP00000374653.4:p.Arg1260Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4757G>T
  hgvsp: ENSP00000346467.3:p.Arg1586Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3776G>T
  hgvsp: ENSP00000384091.1:p.Arg1259Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3611G>T
  hgvsp: ENSP00000384373.1:p.Arg1204Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3617G>T
  hgvsp: ENSP00000385359.1:p.Arg1206Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4754G>T
  hgvsp: ENSP00000386043.2:p.Arg1585Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1448G>T
  hgvsp: ENSP00000272273.5:p.Arg483Leu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3650G>T
  hgvsp: ENSP00000393057.2:p.Arg1217Leu
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6959
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5147
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg1585Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

2-33614294-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614294
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614294
    reference: chr 2
allele count: 18
allele frequency: 1.5193463434398e-4
allele num: 118472
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4755G>C
  hgvsp: ENST00000404816.2:c.4755G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3651G>C
  hgvsp: ENST00000418533.2:c.3651G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3780G>C
  hgvsp: ENST00000390003.4:c.3780G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4758G>C
  hgvsp: ENST00000354476.3:c.4758G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1449G>C
  hgvsp: ENST00000272273.5:c.1449G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3618G>C
  hgvsp: ENST00000404525.1:c.3618G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3612G>C
  hgvsp: ENST00000402934.1:c.3612G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3777G>C
  hgvsp: ENST00000407925.1:c.3777G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 4732
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4369
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg1585Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-33614300-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614300
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614300
    reference: chr 2
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1455A>G
  hgvsp: ENST00000272273.5:c.1455A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3624A>G
  hgvsp: ENST00000404525.1:c.3624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4764A>G
  hgvsp: ENST00000354476.3:c.4764A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3657A>G
  hgvsp: ENST00000418533.2:c.3657A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3618A>G
  hgvsp: ENST00000402934.1:c.3618A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4761A>G
  hgvsp: ENST00000404816.2:c.4761A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3786A>G
  hgvsp: ENST00000390003.4:c.3786A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3783A>G
  hgvsp: ENST00000407925.1:c.3783A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7296
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5601
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48351
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1295
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro1587Pro
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

2-33614307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614307
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614307
    reference: chr 2
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3793C>T
  hgvsp: ENSP00000374653.4:p.Arg1265Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3664C>T
  hgvsp: ENSP00000393057.2:p.Arg1222Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3790C>T
  hgvsp: ENSP00000384091.1:p.Arg1264Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4771C>T
  hgvsp: ENSP00000346467.3:p.Arg1591Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3631C>T
  hgvsp: ENSP00000385359.1:p.Arg1211Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3625C>T
  hgvsp: ENSP00000384373.1:p.Arg1209Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4768C>T
  hgvsp: ENSP00000386043.2:p.Arg1590Trp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1462C>T
  hgvsp: ENSP00000272273.5:p.Arg488Trp
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2952
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7297
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg1590Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

2-33614312-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614312
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614312
    reference: chr 2
allele count: 3
allele frequency: 2.471210398853358e-5
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4776C>T
  hgvsp: ENST00000354476.3:c.4776C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3630C>T
  hgvsp: ENST00000402934.1:c.3630C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1467C>T
  hgvsp: ENST00000272273.5:c.1467C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4773C>T
  hgvsp: ENST00000404816.2:c.4773C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3669C>T
  hgvsp: ENST00000418533.2:c.3669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3636C>T
  hgvsp: ENST00000404525.1:c.3636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3798C>T
  hgvsp: ENST00000390003.4:c.3798C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3795C>T
  hgvsp: ENST00000407925.1:c.3795C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48351
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp1591Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-33614313-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614313
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614313
    reference: chr 2
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3799G>A
  hgvsp: ENSP00000374653.4:p.Ala1267Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3637G>A
  hgvsp: ENSP00000385359.1:p.Ala1213Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3670G>A
  hgvsp: ENSP00000393057.2:p.Ala1224Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4777G>A
  hgvsp: ENSP00000346467.3:p.Ala1593Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3796G>A
  hgvsp: ENSP00000384091.1:p.Ala1266Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4774G>A
  hgvsp: ENSP00000386043.2:p.Ala1592Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1468G>A
  hgvsp: ENSP00000272273.5:p.Ala490Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3631G>A
  hgvsp: ENSP00000384373.1:p.Ala1211Thr
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7297
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala1592Thr
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

2-33614314-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614314
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614314
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1469C>G
  hgvsp: ENSP00000272273.5:p.Ala490Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3638C>G
  hgvsp: ENSP00000385359.1:p.Ala1213Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3632C>G
  hgvsp: ENSP00000384373.1:p.Ala1211Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3797C>G
  hgvsp: ENSP00000384091.1:p.Ala1266Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3800C>G
  hgvsp: ENSP00000374653.4:p.Ala1267Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4778C>G
  hgvsp: ENSP00000346467.3:p.Ala1593Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4775C>G
  hgvsp: ENSP00000386043.2:p.Ala1592Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3671C>G
  hgvsp: ENSP00000393057.2:p.Ala1224Gly
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala1592Gly
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

2-33614316-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614316
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614316
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3673T>G
  hgvsp: ENSP00000393057.2:p.Leu1225Val
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1471T>G
  hgvsp: ENSP00000272273.5:p.Leu491Val
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3799T>G
  hgvsp: ENSP00000384091.1:p.Leu1267Val
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4777T>G
  hgvsp: ENSP00000386043.2:p.Leu1593Val
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3640T>G
  hgvsp: ENSP00000385359.1:p.Leu1214Val
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4780T>G
  hgvsp: ENSP00000346467.3:p.Leu1594Val
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3634T>G
  hgvsp: ENSP00000384373.1:p.Leu1212Val
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3802T>G
  hgvsp: ENSP00000374653.4:p.Leu1268Val
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7294
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu1593Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

2-33614336-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614336
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614336
    reference: chr 2
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4800G>A
  hgvsp: ENST00000354476.3:c.4800G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3819G>A
  hgvsp: ENST00000407925.1:c.3819G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3654G>A
  hgvsp: ENST00000402934.1:c.3654G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3660G>A
  hgvsp: ENST00000404525.1:c.3660G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4797G>A
  hgvsp: ENST00000404816.2:c.4797G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3693G>A
  hgvsp: ENST00000418533.2:c.3693G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1491G>A
  hgvsp: ENST00000272273.5:c.1491G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3822G>A
  hgvsp: ENST00000390003.4:c.3822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7293
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48348
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln1599Gln
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: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum

2-33614338-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614338
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614338
    reference: chr 2
allele count: 1
allele frequency: 8.237232289950576e-6
allele num: 121400
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1493A>G
  hgvsp: ENSP00000272273.5:p.Tyr498Cys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4802A>G
  hgvsp: ENSP00000346467.3:p.Tyr1601Cys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3824A>G
  hgvsp: ENSP00000374653.4:p.Tyr1275Cys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3821A>G
  hgvsp: ENSP00000384091.1:p.Tyr1274Cys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3695A>G
  hgvsp: ENSP00000393057.2:p.Tyr1232Cys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3662A>G
  hgvsp: ENSP00000385359.1:p.Tyr1221Cys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4799A>G
  hgvsp: ENSP00000386043.2:p.Tyr1600Cys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3656A>G
  hgvsp: ENSP00000384373.1:p.Tyr1219Cys
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3705
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7293
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5591
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48348
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Tyr1600Cys
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

2-33614340-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614340
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614340
    reference: chr 2
allele count: 21
allele frequency: 1.729847279197351e-4
allele num: 121398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3664A>G
  hgvsp: ENSP00000385359.1:p.Thr1222Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3823A>G
  hgvsp: ENSP00000384091.1:p.Thr1275Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3697A>G
  hgvsp: ENSP00000393057.2:p.Thr1233Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3826A>G
  hgvsp: ENSP00000374653.4:p.Thr1276Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1495A>G
  hgvsp: ENSP00000272273.5:p.Thr499Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4804A>G
  hgvsp: ENSP00000346467.3:p.Thr1602Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3658A>G
  hgvsp: ENSP00000384373.1:p.Thr1220Ala
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4801A>G
  hgvsp: ENSP00000386043.2:p.Thr1601Ala
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7296
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr1601Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

2-33614340-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614340
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614340
    reference: chr 2
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1495A>T
  hgvsp: ENSP00000272273.5:p.Thr499Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3826A>T
  hgvsp: ENSP00000374653.4:p.Thr1276Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3664A>T
  hgvsp: ENSP00000385359.1:p.Thr1222Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3658A>T
  hgvsp: ENSP00000384373.1:p.Thr1220Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3823A>T
  hgvsp: ENSP00000384091.1:p.Thr1275Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4801A>T
  hgvsp: ENSP00000386043.2:p.Thr1601Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4804A>T
  hgvsp: ENSP00000346467.3:p.Thr1602Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3697A>T
  hgvsp: ENSP00000393057.2:p.Thr1233Ser
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3516
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5133
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7296
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2878
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 789
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr1601Ser
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum

2-33614342-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614342
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614342
    reference: chr 2
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3666T>C
  hgvsp: ENST00000404525.1:c.3666T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3825T>C
  hgvsp: ENST00000407925.1:c.3825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3828T>C
  hgvsp: ENST00000390003.4:c.3828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4803T>C
  hgvsp: ENST00000404816.2:c.4803T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1497T>C
  hgvsp: ENST00000272273.5:c.1497T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4806T>C
  hgvsp: ENST00000354476.3:c.4806T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3660T>C
  hgvsp: ENST00000402934.1:c.3660T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3699T>C
  hgvsp: ENST00000418533.2:c.3699T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7292
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr1601Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: T
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-33614343-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614343
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614343
    reference: chr 2
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3667C>A
  hgvsp: ENSP00000385359.1:p.Pro1223Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3700C>A
  hgvsp: ENSP00000393057.2:p.Pro1234Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4807C>A
  hgvsp: ENSP00000346467.3:p.Pro1603Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3829C>A
  hgvsp: ENSP00000374653.4:p.Pro1277Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1498C>A
  hgvsp: ENSP00000272273.5:p.Pro500Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3661C>A
  hgvsp: ENSP00000384373.1:p.Pro1221Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4804C>A
  hgvsp: ENSP00000386043.2:p.Pro1602Thr
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3826C>A
  hgvsp: ENSP00000384091.1:p.Pro1276Thr
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7291
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro1602Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-33614344-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614344
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614344
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3662C>A
  hgvsp: ENSP00000384373.1:p.Pro1221Gln
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3701C>A
  hgvsp: ENSP00000393057.2:p.Pro1234Gln
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3827C>A
  hgvsp: ENSP00000384091.1:p.Pro1276Gln
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1499C>A
  hgvsp: ENSP00000272273.5:p.Pro500Gln
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4808C>A
  hgvsp: ENSP00000346467.3:p.Pro1603Gln
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3668C>A
  hgvsp: ENSP00000385359.1:p.Pro1223Gln
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4805C>A
  hgvsp: ENSP00000386043.2:p.Pro1602Gln
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3830C>A
  hgvsp: ENSP00000374653.4:p.Pro1277Gln
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4766
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7291
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro1602Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

2-33614346-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614346
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614346
    reference: chr 2
allele count: 86
allele frequency: 7.207750846491669e-4
allele num: 119316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3703G>A
  hgvsp: ENSP00000393057.2:p.Glu1235Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1501G>A
  hgvsp: ENSP00000272273.5:p.Glu501Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3670G>A
  hgvsp: ENSP00000385359.1:p.Glu1224Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3664G>A
  hgvsp: ENSP00000384373.1:p.Glu1222Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3829G>A
  hgvsp: ENSP00000384091.1:p.Glu1277Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3832G>A
  hgvsp: ENSP00000374653.4:p.Glu1278Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4810G>A
  hgvsp: ENSP00000346467.3:p.Glu1604Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4807G>A
  hgvsp: ENSP00000386043.2:p.Glu1603Lys
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2877
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7678
  bin: 9.75e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5098
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 3
hgvs: p.Glu1603Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

2-33614348-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614348
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614348
    reference: chr 2
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3672A>T
  hgvsp: ENSP00000385359.1:p.Glu1224Asp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4809A>T
  hgvsp: ENSP00000386043.2:p.Glu1603Asp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3831A>T
  hgvsp: ENSP00000384091.1:p.Glu1277Asp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3666A>T
  hgvsp: ENSP00000384373.1:p.Glu1222Asp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3834A>T
  hgvsp: ENSP00000374653.4:p.Glu1278Asp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3705A>T
  hgvsp: ENSP00000393057.2:p.Glu1235Asp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4812A>T
  hgvsp: ENSP00000346467.3:p.Glu1604Asp
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1503A>T
  hgvsp: ENSP00000272273.5:p.Glu501Asp
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7310
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu1603Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

2-33614352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614352
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614352
    reference: chr 2
allele count: 4
allele frequency: 3.295218637756615e-5
allele num: 121388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4816G>A
  hgvsp: ENSP00000346467.3:p.Asp1606Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1507G>A
  hgvsp: ENSP00000272273.5:p.Asp503Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3709G>A
  hgvsp: ENSP00000393057.2:p.Asp1237Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3670G>A
  hgvsp: ENSP00000384373.1:p.Asp1224Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3676G>A
  hgvsp: ENSP00000385359.1:p.Asp1226Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3838G>A
  hgvsp: ENSP00000374653.4:p.Asp1280Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3835G>A
  hgvsp: ENSP00000384091.1:p.Asp1279Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4813G>A
  hgvsp: ENSP00000386043.2:p.Asp1605Asn
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7311
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp1605Asn
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

2-33614354-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614354
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614354
    reference: chr 2
allele count: 13
allele frequency: 1.070981348447901e-4
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1509T>A
  hgvsp: ENSP00000272273.5:p.Asp503Glu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3672T>A
  hgvsp: ENSP00000384373.1:p.Asp1224Glu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3678T>A
  hgvsp: ENSP00000385359.1:p.Asp1226Glu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3711T>A
  hgvsp: ENSP00000393057.2:p.Asp1237Glu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4818T>A
  hgvsp: ENSP00000346467.3:p.Asp1606Glu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3837T>A
  hgvsp: ENSP00000384091.1:p.Asp1279Glu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4815T>A
  hgvsp: ENSP00000386043.2:p.Asp1605Glu
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3840T>A
  hgvsp: ENSP00000374653.4:p.Asp1280Glu
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5076
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4401
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7312
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 5546
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp1605Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

2-33614358-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614358
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614358
    reference: chr 2
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3715T>A
  hgvsp: ENSP00000393057.2:p.Tyr1239Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3844T>A
  hgvsp: ENSP00000374653.4:p.Tyr1282Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4822T>A
  hgvsp: ENSP00000346467.3:p.Tyr1608Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3682T>A
  hgvsp: ENSP00000385359.1:p.Tyr1228Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4819T>A
  hgvsp: ENSP00000386043.2:p.Tyr1607Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3676T>A
  hgvsp: ENSP00000384373.1:p.Tyr1226Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1513T>A
  hgvsp: ENSP00000272273.5:p.Tyr505Asn
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3841T>A
  hgvsp: ENSP00000384091.1:p.Tyr1281Asn
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48514
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr1607Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ

2-33614366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614366
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614366
    reference: chr 2
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4827C>T
  hgvsp: ENST00000404816.2:c.4827C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3690C>T
  hgvsp: ENST00000404525.1:c.3690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3723C>T
  hgvsp: ENST00000418533.2:c.3723C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4830C>T
  hgvsp: ENST00000354476.3:c.4830C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3849C>T
  hgvsp: ENST00000407925.1:c.3849C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3852C>T
  hgvsp: ENST00000390003.4:c.3852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3684C>T
  hgvsp: ENST00000402934.1:c.3684C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1521C>T
  hgvsp: ENST00000272273.5:c.1521C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1084
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1265
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ile1609Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ

2-33614374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614374
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614374
    reference: chr 2
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3730+1G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4837+1G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3691+1G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4834+1G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3697+1G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3856+1G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3859+1G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1528+1G>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 9.25e1
  variant carriers: 0
hgvs: c.4834+1G>A
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

2-33614386-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614386
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614386
    reference: chr 2
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4834+13A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1528+13A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3691+13A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3859+13A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3730+13A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4837+13A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3697+13A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3856+13A>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5078
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4897
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1560
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/2-33614387-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614387
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614387
    reference: chr 2
allele count: 2
allele frequency: 1.650628063978344e-5
allele num: 121166
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4837+14C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3859+14C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3691+14C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3730+14C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3697+14C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3856+14C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1528+14C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4834+14C>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

2-33614394-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614394
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614394
    reference: chr 2
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3859+21C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3730+21C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3697+21C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1528+21C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3856+21C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4834+21C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4837+21C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3691+21C>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-33614402-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614402
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614402
    reference: chr 2
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3697+29A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4837+29A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3730+29A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4834+29A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3856+29A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3859+29A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1528+29A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3691+29A>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4234
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3768
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1070
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

2-33614424-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614424
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614424
    reference: chr 2
allele count: 2
allele frequency: 1.65576620581174e-5
allele num: 120790
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4834+51A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1528+51A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3730+51A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3697+51A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3856+51A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4837+51A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3691+51A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3859+51A>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

2-33614425-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33614425
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33614425
    reference: chr 2
allele count: 1
allele frequency: 8.28775070445881e-6
allele num: 120660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3697+52T>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3856+52T>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4837+52T>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3859+52T>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3730+52T>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3691+52T>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1528+52T>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4834+52T>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4233
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2295
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4402
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1044
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

2-33622152-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622152
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622152
    reference: chr 2
allele count: 1
allele frequency: 1.073606458816456e-5
allele num: 93144
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-48A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-48A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-48A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-48A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-48A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-48A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-48A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-48A>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20067
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4803
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8609
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2512
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP

2-33622153-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622153
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622153
    reference: chr 2
allele count: 54
allele frequency: 5.79051213862915e-4
allele num: 93256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-47T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-47T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-47T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-47T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-47T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-47T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-47T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-47T>C
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12241
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20048
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 1.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8592
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4896
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4841
  bin: 9.75e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 7442
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2073
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1588
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD

2-33622156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622156
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622156
    reference: chr 2
allele count: 1
allele frequency: 1.068855683105667e-5
allele num: 93558
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-44G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-44G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-44G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-44G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-44G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-44G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-44G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-44G>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10950
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

2-33622164-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622164
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622164
    reference: chr 2
allele count: 1
allele frequency: 1.055498089548458e-5
allele num: 94742
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-36G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-36G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-36G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-36G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-36G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-36G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-36G>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-36G>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5066
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3171
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4815
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4613
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1754
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

2-33622166-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622166
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622166
    reference: chr 2
allele count: 1
allele frequency: 1.050155423002604e-5
allele num: 95224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-34A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-34A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-34A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-34A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-34A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-34A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-34A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-34A>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4486
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5107
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12151
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

2-33622170-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622170
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622170
    reference: chr 2
allele count: 2
allele frequency: 2.07507625905252e-5
allele num: 96382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-30C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-30C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-30C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-30C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-30C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-30C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-30C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-30C>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11834
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4831
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 11891
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-33622172-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622172
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622172
    reference: chr 2
allele count: 1
allele frequency: 1.030078285949732e-5
allele num: 97080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-28A>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-28A>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-28A>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-28A>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-28A>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-28A>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-28A>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-28A>C
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3826
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3318
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21844
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11657
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

2-33622172-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622172
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622172
    reference: chr 2
allele count: 4
allele frequency: 4.120313143798929e-5
allele num: 97080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-28A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-28A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-28A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-28A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-28A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-28A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-28A>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-28A>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3954
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12346
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11563
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21844
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3318
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4838
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP

2-33622182-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622182
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622181
    reference: chr 2
allele count: 2
allele frequency: 1.958978980155543e-5
allele num: 102094
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-17delT
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-17delT
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-17delT
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-17delT
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-17delT
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-17delT
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-17delT
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-17delT
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30591
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3261
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28481
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9494
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: CT
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-33622184-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622184
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622184
    reference: chr 2
allele count: 1
allele frequency: 9.666692444513185e-6
allele num: 103448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-16G>T
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-16G>T
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-16G>T
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-16G>T
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-16G>T
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-16G>T
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-16G>T
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-16G>T
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8844
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30463
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/2-33622185-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622185
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622185
    reference: chr 2
allele count: 2
allele frequency: 1.918686083769834e-5
allele num: 104238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-15C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-15C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-15C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-15C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-15C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-15C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-15C>A
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-15C>A
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32403
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30758
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3679
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8512
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

2-33622191-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622191
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622191
    reference: chr 2
allele count: 12
allele frequency: 1.112079031749856e-4
allele num: 107906
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-9C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-9C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-9C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-9C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-9C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-9C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-9C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-9C>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6609
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35134
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6739
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1050
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4196
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

2-33622195-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622195
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622195
    reference: chr 2
allele count: 2
allele frequency: 1.815277374382806e-5
allele num: 110176
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-5T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-5T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-5T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-5T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-5T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-5T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-5T>C
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-5T>C
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7037
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35383
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1171
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4446
  bin: 6.75e1
  variant carriers: 0
hgvs: c.4835-5T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

2-33622196-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622196
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622196
    reference: chr 2
allele count: 1
allele frequency: 9.033097268391387e-6
allele num: 110704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3857-4C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1529-4C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3860-4C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4835-4C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3698-4C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4838-4C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3731-4C>G
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3692-4C>G
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37030
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4884
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36017
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
hgvs: c.4835-4C>G
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

2-33622209-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622209
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622209
    reference: chr 2
allele count: 1
allele frequency: 8.614006374364718e-6
allele num: 116090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3866A>G
  hgvsp: ENSP00000384091.1:p.Asn1289Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3707A>G
  hgvsp: ENSP00000385359.1:p.Asn1236Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4844A>G
  hgvsp: ENSP00000386043.2:p.Asn1615Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1538A>G
  hgvsp: ENSP00000272273.5:p.Asn513Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3701A>G
  hgvsp: ENSP00000384373.1:p.Asn1234Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3869A>G
  hgvsp: ENSP00000374653.4:p.Asn1290Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3740A>G
  hgvsp: ENSP00000393057.2:p.Asn1247Ser
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4847A>G
  hgvsp: ENSP00000346467.3:p.Asn1616Ser
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39225
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn1615Ser
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

2-33622211-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622211
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622211
    reference: chr 2
allele count: 2
allele frequency: 1.714648239913582e-5
allele num: 116642
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4846A>G
  hgvsp: ENSP00000386043.2:p.Ser1616Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4849A>G
  hgvsp: ENSP00000346467.3:p.Ser1617Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3742A>G
  hgvsp: ENSP00000393057.2:p.Ser1248Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3709A>G
  hgvsp: ENSP00000385359.1:p.Ser1237Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3871A>G
  hgvsp: ENSP00000374653.4:p.Ser1291Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3703A>G
  hgvsp: ENSP00000384373.1:p.Ser1235Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1540A>G
  hgvsp: ENSP00000272273.5:p.Ser514Gly
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3868A>G
  hgvsp: ENSP00000384091.1:p.Ser1290Gly
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8531
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39105
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1320
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5181
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser1616Gly
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-33622222-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622222
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622222
    reference: chr 2
allele count: 1
allele frequency: 8.406045628015669e-6
allele num: 118962
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3753G>A
  hgvsp: ENST00000418533.2:c.3753G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3714G>A
  hgvsp: ENST00000402934.1:c.3714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1551G>A
  hgvsp: ENST00000272273.5:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4857G>A
  hgvsp: ENST00000404816.2:c.4857G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4860G>A
  hgvsp: ENST00000354476.3:c.4860G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3720G>A
  hgvsp: ENST00000404525.1:c.3720G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3882G>A
  hgvsp: ENST00000390003.4:c.3882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3879G>A
  hgvsp: ENST00000407925.1:c.3879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40116
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4928
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu1619Glu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/2-33622227-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622227
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622227
    reference: chr 2
allele count: 2
allele frequency: 1.671095068598453e-5
allele num: 119682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3719A>C
  hgvsp: ENSP00000384373.1:p.Gln1240Pro
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4865A>C
  hgvsp: ENSP00000346467.3:p.Gln1622Pro
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3884A>C
  hgvsp: ENSP00000384091.1:p.Gln1295Pro
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3887A>C
  hgvsp: ENSP00000374653.4:p.Gln1296Pro
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3758A>C
  hgvsp: ENSP00000393057.2:p.Gln1253Pro
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4862A>C
  hgvsp: ENSP00000386043.2:p.Gln1621Pro
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3725A>C
  hgvsp: ENSP00000385359.1:p.Gln1242Pro
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1556A>C
  hgvsp: ENSP00000272273.5:p.Gln519Pro
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9811
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4937
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln1621Pro
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: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

2-33622232-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622232
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622232
    reference: chr 2
allele count: 1
allele frequency: 8.319605983460623e-6
allele num: 120198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3763G>A
  hgvsp: ENSP00000393057.2:p.Glu1255Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3730G>A
  hgvsp: ENSP00000385359.1:p.Glu1244Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3724G>A
  hgvsp: ENSP00000384373.1:p.Glu1242Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3889G>A
  hgvsp: ENSP00000384091.1:p.Glu1297Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4870G>A
  hgvsp: ENSP00000346467.3:p.Glu1624Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3892G>A
  hgvsp: ENSP00000374653.4:p.Glu1298Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1561G>A
  hgvsp: ENSP00000272273.5:p.Glu521Lys
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4867G>A
  hgvsp: ENSP00000386043.2:p.Glu1623Lys
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1548
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu1623Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

2-33622234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33622234
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 33622234
    reference: chr 2
allele count: 1
allele frequency: 8.311999202048076e-6
allele num: 120308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000385359
  ensembl transcript: ENST00000404525
  gene symbol: LTBP1
  hgvsc: ENST00000404525.1:c.3732G>A
  hgvsp: ENST00000404525.1:c.3732G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000386043
  ensembl transcript: ENST00000404816
  gene symbol: LTBP1
  hgvsc: ENST00000404816.2:c.4869G>A
  hgvsp: ENST00000404816.2:c.4869G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000272273
  ensembl transcript: ENST00000272273
  gene symbol: LTBP1
  hgvsc: ENST00000272273.5:c.1563G>A
  hgvsp: ENST00000272273.5:c.1563G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000346467
  ensembl transcript: ENST00000354476
  gene symbol: LTBP1
  hgvsc: ENST00000354476.3:c.4872G>A
  hgvsp: ENST00000354476.3:c.4872G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000393057
  ensembl transcript: ENST00000418533
  gene symbol: LTBP1
  hgvsc: ENST00000418533.2:c.3765G>A
  hgvsp: ENST00000418533.2:c.3765G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000374653
  ensembl transcript: ENST00000390003
  gene symbol: LTBP1
  hgvsc: ENST00000390003.4:c.3894G>A
  hgvsp: ENST00000390003.4:c.3894G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384373
  ensembl transcript: ENST00000402934
  gene symbol: LTBP1
  hgvsc: ENST00000402934.1:c.3726G>A
  hgvsp: ENST00000402934.1:c.3726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000049323
  ensembl protein: ENSP00000384091
  ensembl transcript: ENST00000407925
  gene symbol: LTBP1
  hgvsc: ENST00000407925.1:c.3891G>A
  hgvsp: ENST00000407925.1:c.3891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6714
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39797
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu1623Glu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 48295
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1304
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1270
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.301868239921337e-4
allele num: 16272
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.179e1

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

DP
type: SiteQuality
SIO_000300: 3.968299e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 1.296e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1117
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16314
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: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 3.364e0

MQ
type: SiteQuality
SIO_000300: 5.987e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-2

DP
type: SiteQuality
SIO_000300: 3.970157e6

QD
type: SiteQuality
SIO_000300: 1.286e1

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1119
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48290
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 779
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1279
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
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: 16324
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: 900
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.43e-1

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

FS
type: SiteQuality
SIO_000300: 6.63e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.548e0

DP
type: SiteQuality
SIO_000300: 3.970456e6

GenotypeQuality
all individuals: 780
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1298
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1287
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.75e1
variant carriers: 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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16374
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

DP
type: SiteQuality
SIO_000300: 3.973386e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 3.235e0

VQSLOD
type: SiteQuality
SIO_000300: -9.379999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

QD
type: SiteQuality
SIO_000300: 1.407e1

MQ
type: SiteQuality
SIO_000300: 5.889e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.198e0

GenotypeQuality
all individuals: 1295
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 780
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1593
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
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: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.338e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 1.566e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 3.975568e6

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 779
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5351
bin: 6.25e1
variant carriers: 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: 8652
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

FS
type: SiteQuality
SIO_000300: 1.388e0

MQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
SIO_000300: 3.976235e6

QD
type: SiteQuality
SIO_000300: 1.194e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.091e0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 782
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 9.25e1
variant carriers: 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: 1
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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VQSLOD
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ReadPosRankSum
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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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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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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DP
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FS
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VQSLOD
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8650
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Latino
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allele frequency: 0.0e0
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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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European (Finnish)
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

Latino
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allele num: 11578
num of homozygotes: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele num: 6614
num of homozygotes: 0

East Asian
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MQ
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BaseQRankSum
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QD
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ClippingRankSum
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FS
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VQSLOD
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DP
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InbreedingCoeff
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MQRankSum
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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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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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African
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66710
num of homozygotes: 0

Other
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num of homozygotes: 0

FS
type: SiteQuality
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

East Asian
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Other
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African
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allele frequency: 1.057285659361784e-3
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European (Finnish)
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European (Non-Finnish)
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South Asian
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FS
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

African
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allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
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: 16512
num of homozygotes: 0

European (Finnish)
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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: 8648
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.21e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 3.978368e6

QD
type: SiteQuality
SIO_000300: 1.37e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele 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: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 6.391e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.353e1

DP
type: SiteQuality
SIO_000300: 3.978336e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
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
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.101e0

VQSLOD
type: SiteQuality
SIO_000300: 8.53e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

DP
type: SiteQuality
SIO_000300: 3.978351e6

QD
type: SiteQuality
SIO_000300: 1.327e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.921968095329617e-4
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
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: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.327e1

VQSLOD
type: SiteQuality
SIO_000300: 8.53e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.34e-1

DP
type: SiteQuality
SIO_000300: 3.978351e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.101e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495729057395475e-5
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

FS
type: SiteQuality
SIO_000300: 4.024e0

DP
type: SiteQuality
SIO_000300: 3.977822e6

QD
type: SiteQuality
SIO_000300: 1.376e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 2
allele frequency: 2.312138728323699e-4
allele num: 8650
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.953e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.62e-1

FS
type: SiteQuality
SIO_000300: 5.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.09e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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: 11576
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.389e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.884e0

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.43e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.060999999999999e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.193e0

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.939e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele num: 16512
num of homozygotes: 0

African
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East Asian
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allele frequency: 4.625346901017577e-4
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

Other
type: Population
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allele num: 908
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

Latino
type: Population
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allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
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FS
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 3.977421e6

MQRankSum
type: SiteQuality
SIO_000300: 6.16e-1

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 80
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1237
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1251
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1528
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46599
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.154442768766735e-4
allele num: 64982
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.044153720359771e-4
allele num: 9784
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.604621309370988e-4
allele num: 6232
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.164e0

QD
type: SiteQuality
SIO_000300: 5.0e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.288e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.47e-1

FS
type: SiteQuality
SIO_000300: 2.17477e2

MQ
type: SiteQuality
SIO_000300: 5.833e1

DP
type: SiteQuality
SIO_000300: 4.011706e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.407e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e0

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

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 790
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 691
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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.183e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 7.915e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.52e0

VQSLOD
type: SiteQuality
SIO_000300: -3.112e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

DP
type: SiteQuality
SIO_000300: 4.008426e6

GenotypeQuality
all individuals: 5601
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1296
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variant carriers: 0

GenotypeQuality
all individuals: 1277
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variant carriers: 0

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

GenotypeQuality
all individuals: 689
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1101
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variant carriers: 0

GenotypeQuality
all individuals: 48352
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variant carriers: 1

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

GenotypeQuality
all individuals: 1578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 8648
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: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.195000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 4.008347e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.62e-1

MQ
type: SiteQuality
SIO_000300: 5.778e1

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 789
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 5599
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variant carriers: 0

GenotypeQuality
all individuals: 691
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variant carriers: 0

GenotypeQuality
all individuals: 1579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
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: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
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: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 4.008384e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-3

FS
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-2

GenotypeQuality
all individuals: 691
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
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variant carriers: 0

GenotypeQuality
all individuals: 1580
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5600
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48350
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1275
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.313743637204998e-4
allele num: 8644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 5.788e0

MQRankSum
type: SiteQuality
SIO_000300: 8.57e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

DP
type: SiteQuality
SIO_000300: 4.008243e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

GenotypeQuality
all individuals: 788
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5594
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48350
bin: 9.75e1
variant carriers: 1

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

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

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

GenotypeQuality
all individuals: 4
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1101
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 691
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1297
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 9.25e1
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: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
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: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 3.229e1

DP
type: SiteQuality
SIO_000300: 4.00813e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.76e-1

FS
type: SiteQuality
SIO_000300: 1.586e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.18e0

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

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

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

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 48349
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1275
bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 1580
bin: 9.25e1
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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

VQSLOD
type: SiteQuality
SIO_000300: -2.056e-1

QD
type: SiteQuality
SIO_000300: 1.283e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.613e0

DP
type: SiteQuality
SIO_000300: 4.008102e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

FS
type: SiteQuality
SIO_000300: 8.260999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 693
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1102
bin: 7.75e1
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GenotypeQuality
all individuals: 788
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variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1296
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5592
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 908
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

DP
type: SiteQuality
SIO_000300: 4.008004e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.651e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.733e1

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 14
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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
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1103
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
all individuals: 1579
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variant carriers: 0

GenotypeQuality
all individuals: 1275
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.008055e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.519e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.092e0

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

BaseQRankSum
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SIO_000300: 4.77e0

VQSLOD
type: SiteQuality
SIO_000300: 9.599999999999999e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 21

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

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.491983577571999e-5
allele num: 66738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.455425017277125e-4
allele num: 11576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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South Asian
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allele count: 11
allele frequency: 6.661821705426356e-4
allele num: 16512
num of homozygotes: 0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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BaseQRankSum
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SIO_000300: 3.17e0

VQSLOD
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FS
type: SiteQuality
SIO_000300: 1.097e0

InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.94e1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.097e0

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

DP
type: SiteQuality
SIO_000300: 4.008683e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.388e1

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
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: 8644
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 4.007803e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.615e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.29e0

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.007817e6

MQRankSum
type: SiteQuality
SIO_000300: 3.38e-1

FS
type: SiteQuality
SIO_000300: 2.785e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 1.379e1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.788e0

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

European (Finnish)
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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.318e0

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

ClippingRankSum
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QD
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 4.007877e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 54

European (Non-Finnish)
type: Population
allele count: 56
allele frequency: 8.548313234620668e-4
allele num: 65510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.319647413593134e-4
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 22
allele frequency: 2.226269985832827e-3
allele num: 9882
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.126126126126126e-3
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.283380458686773e-4
allele num: 6366
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.864e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.112e0

FS
type: SiteQuality
SIO_000300: 1.71039e2

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

QD
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.917e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

FS
type: SiteQuality
SIO_000300: 3.311e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

QD
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.312673450508788e-4
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.291e1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 762
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
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

African
type: Population
allele count: 13
allele frequency: 1.249279261964251e-3
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
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: -9.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.93e0

DP
type: SiteQuality
SIO_000300: 4.017824e6

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
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

FS
type: SiteQuality
SIO_000300: 6.07e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.009e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

DP
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SIO_000300: 4.016971e6

VQSLOD
type: SiteQuality
SIO_000300: -2.27e-2

QD
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SIO_000300: 1.448e1

MQ
type: SiteQuality
SIO_000300: 5.907e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
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: 8646
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.011e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.067e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

DP
type: SiteQuality
SIO_000300: 4.01634e6

FS
type: SiteQuality
SIO_000300: 5.632e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16468
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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

DP
type: SiteQuality
SIO_000300: 4.014946e6

VQSLOD
type: SiteQuality
SIO_000300: 7.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.93e0

FS
type: SiteQuality
SIO_000300: 6.245e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.213e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.352e1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 1.500285054160291e-5
allele num: 66654
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.010308e6

MQ
type: SiteQuality
SIO_000300: 5.784e1

QD
type: SiteQuality
SIO_000300: 1.831e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.81e-1

GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1260
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001290554938624e-5
allele num: 66638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
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: 8642
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.942e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.49e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

South Asian
type: Population
allele count: 0
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allele num: 16344
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.648e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.895e1

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

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

South Asian
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allele count: 0
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MQ
type: SiteQuality
SIO_000300: 5.829e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.01e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

East Asian
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African
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allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005259203606311e-5
allele num: 66550
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.972e1

DP
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SIO_000300: 3.98585e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.246096189881324e-5
allele num: 16010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.82e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 3.986157e6

FS
type: SiteQuality
SIO_000300: 3.676e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.663e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.498e1

VQSLOD
type: SiteQuality
SIO_000300: 2.36e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7950
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.980119599223793e-5
allele num: 50502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQ
type: SiteQuality
SIO_000300: 5.938e1

VQSLOD
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SIO_000300: 2.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

QD
type: SiteQuality
SIO_000300: 1.082e1

DP
type: SiteQuality
SIO_000300: 1.155017e6

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

African
type: Population
allele count: 47
allele frequency: 5.497076023391813e-3
allele num: 8550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.99895036737142e-4
allele num: 13338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.932136360041129e-5
allele num: 50572
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 1.542e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

FS
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.158837e6

VQSLOD
type: SiteQuality
SIO_000300: 3.93e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5608
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.972075412163761e-5
allele num: 50708
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8006
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.0e-1

FS
type: SiteQuality
SIO_000300: 4.336e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.978e0

DP
type: SiteQuality
SIO_000300: 1.173814e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 1.95e0

QD
type: SiteQuality
SIO_000300: 9.029999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.749e-1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8706
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.225790634959549e-4
allele num: 8158
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5674
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.229979e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.764e0

QD
type: SiteQuality
SIO_000300: 1.234e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51656
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5684
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.358351729212656e-5
allele num: 13590
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.249768e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

FS
type: SiteQuality
SIO_000300: 1.497e0

VQSLOD
type: SiteQuality
SIO_000300: 3.55e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.564e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6706
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.458363715910748e-4
allele num: 13714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5732
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.292141e6

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQ
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52770
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.123848055742864e-4
allele num: 8898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13774
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.37e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.534e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-2

DP
type: SiteQuality
SIO_000300: 1.313637e6

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52770
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
type: Population
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allele frequency: 2.904022070567736e-4
allele num: 13774
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8898
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.37e-1

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.98e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 335
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 469
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9210
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.398797034550287e-4
allele num: 14298
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9094
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5930
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.069e1

FS
type: SiteQuality
SIO_000300: 3.647e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.12e-1

DP
type: SiteQuality
SIO_000300: 1.414574e6

MQ
type: SiteQuality
SIO_000300: 6.054e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 2.75e1
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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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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.76878449129758e-5
allele num: 56536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14402
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.041e0

VQSLOD
type: SiteQuality
SIO_000300: 7.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.515e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.95e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.34e-1

QD
type: SiteQuality
SIO_000300: 1.509e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.508156463778284e-5
allele num: 57010
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6018
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.513e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

FS
type: SiteQuality
SIO_000300: 3.418e0

QD
type: SiteQuality
SIO_000300: 1.016e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.63e-1

DP
type: SiteQuality
SIO_000300: 1.449456e6

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

GenotypeQuality
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bin: 3.25e1
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: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9528
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.700148508167949e-4
allele num: 14814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

Latino
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: 7480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.350849346526629e-4
allele num: 59222
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.35e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

FS
type: SiteQuality
SIO_000300: 2.783e0

VQSLOD
type: SiteQuality
SIO_000300: 2.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 1.503655e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60572
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.615746795710175e-4
allele num: 7646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

FS
type: SiteQuality
SIO_000300: 9.360000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.533964e6

MQ
type: SiteQuality
SIO_000300: 5.942e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 1.371e1

VQSLOD
type: SiteQuality
SIO_000300: 9.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 77
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GenotypeQuality
all individuals: 5370
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.642036124794745e-5
allele num: 60900
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7680
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.147e0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

QD
type: SiteQuality
SIO_000300: 1.044e1

DP
type: SiteQuality
SIO_000300: 1.542676e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-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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GenotypeQuality
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GenotypeQuality
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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: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.363752068219422e-5
allele num: 15714
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10036
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10902
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

DP
type: SiteQuality
SIO_000300: 1.610803e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.844e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15772
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.109162702484221e-5
allele num: 64326
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.049e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.024e0

QD
type: SiteQuality
SIO_000300: 5.59e0

DP
type: SiteQuality
SIO_000300: 1.618265e6

MQRankSum
type: SiteQuality
SIO_000300: 3.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 275
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.219679064560268e-5
allele num: 16078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65564
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.207e1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.342e0

MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.653755e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.624e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 271
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2324
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40651
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5656
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65924
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.355157795572303e-4
allele num: 8492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.667438e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.85e-1

FS
type: SiteQuality
SIO_000300: 8.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.531e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

QD
type: SiteQuality
SIO_000300: 1.461e1

MQ
type: SiteQuality
SIO_000300: 5.941e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-1

GenotypeQuality
all individuals: 656
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40922
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2423
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5852
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4951
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66178
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.168770453482936e-4
allele num: 8556
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.0e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

MQRankSum
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

FS
type: SiteQuality
SIO_000300: 1.316e0

QD
type: SiteQuality
SIO_000300: 1.121e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.511e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e-2

DP
type: SiteQuality
SIO_000300: 1.676141e6