http://identifiers.org/exac.variant/17-4622675-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622675
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622675
    reference: chr 17
allele count: 2
allele frequency: 1.650410126916539e-5
allele num: 121182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000458371
  ensembl transcript: ENST00000574502
  gene symbol: ARRB2
  hgvsc: ENST00000574502.1:c.*355A>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.301A>C
  hgvsp: ENSP00000460607.1:p.Lys101Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.940A>C
  hgvsp: ENSP00000403701.3:p.Lys314Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.301A>C
  hgvsp: ENSP00000465296.1:p.Lys101Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+91A>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.301A>C
  hgvsp: ENSP00000466344.1:p.Lys101Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.832A>C
  hgvsp: ENSP00000341895.2:p.Lys278Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.877A>C
  hgvsp: ENSP00000269260.2:p.Lys293Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.832A>C
  hgvsp: ENSP00000370898.6:p.Lys278Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465877
  ensembl transcript: ENST00000571428
  gene symbol: ARRB2
  hgvsc: ENST00000571428.1:c.301A>C
  hgvsp: ENSP00000465877.1:p.Lys101Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*168A>C
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9340
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys314Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

17-4622683-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622683
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622683
    reference: chr 17
allele count: 2
allele frequency: 1.65180046250413e-5
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.840G>A
  hgvsp: ENST00000381488.6:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000458371
  ensembl transcript: ENST00000574502
  gene symbol: ARRB2
  hgvsc: ENST00000574502.1:c.*363G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465877
  ensembl transcript: ENST00000571428
  gene symbol: ARRB2
  hgvsc: ENST00000571428.1:c.309G>A
  hgvsp: ENST00000571428.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.840G>A
  hgvsp: ENST00000346341.2:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.885G>A
  hgvsp: ENST00000269260.2:c.885G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.948G>A
  hgvsp: ENST00000412477.3:c.948G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.309G>A
  hgvsp: ENST00000574954.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.309G>A
  hgvsp: ENST00000571206.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+99G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.309G>A
  hgvsp: ENST00000572457.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*176G>A
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5087
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys316Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

17-4622686-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622686
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622686
    reference: chr 17
allele count: 50
allele frequency: 4.131343678217903e-4
allele num: 121026
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.312C>T
  hgvsp: ENST00000574954.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*179C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+102C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.312C>T
  hgvsp: ENST00000571206.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.888C>T
  hgvsp: ENST00000269260.2:c.888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465877
  ensembl transcript: ENST00000571428
  gene symbol: ARRB2
  hgvsc: ENST00000571428.1:c.312C>T
  hgvsp: ENST00000571428.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.312C>T
  hgvsp: ENST00000572457.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.843C>T
  hgvsp: ENST00000346341.2:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.951C>T
  hgvsp: ENST00000412477.3:c.951C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000458371
  ensembl transcript: ENST00000574502
  gene symbol: ARRB2
  hgvsc: ENST00000574502.1:c.*366C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.843C>T
  hgvsp: ENST00000381488.6:c.843C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7282
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13349
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5086
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.His317His
num of homozygotes: 1
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

17-4622687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622687
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622687
    reference: chr 17
allele count: 3
allele frequency: 2.479215906649257e-5
allele num: 121006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.313G>A
  hgvsp: ENSP00000460607.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+103G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.313G>A
  hgvsp: ENSP00000466344.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*180G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.844G>A
  hgvsp: ENSP00000370898.6:p.Glu282Lys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465877
  ensembl transcript: ENST00000571428
  gene symbol: ARRB2
  hgvsc: ENST00000571428.1:c.313G>A
  hgvsp: ENSP00000465877.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.889G>A
  hgvsp: ENSP00000269260.2:p.Glu297Lys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.844G>A
  hgvsp: ENSP00000341895.2:p.Glu282Lys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.313G>A
  hgvsp: ENSP00000465296.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000458371
  ensembl transcript: ENST00000574502
  gene symbol: ARRB2
  hgvsc: ENST00000574502.1:c.*367G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.952G>A
  hgvsp: ENSP00000403701.3:p.Glu318Lys
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13436
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu318Lys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

17-4622689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622689
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622689
    reference: chr 17
allele count: 1
allele frequency: 8.266785708380868e-6
allele num: 120966
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.315G>A
  hgvsp: ENST00000574954.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.891G>A
  hgvsp: ENST00000269260.2:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.846G>A
  hgvsp: ENST00000346341.2:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*182G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.954G>A
  hgvsp: ENST00000412477.3:c.954G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.315G>A
  hgvsp: ENST00000572457.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+105G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465877
  ensembl transcript: ENST00000571428
  gene symbol: ARRB2
  hgvsc: ENST00000571428.1:c.315G>A
  hgvsp: ENST00000571428.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.846G>A
  hgvsp: ENST00000381488.6:c.846G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.315G>A
  hgvsp: ENST00000571206.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000458371
  ensembl transcript: ENST00000574502
  gene symbol: ARRB2
  hgvsc: ENST00000574502.1:c.*369G>A
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3303
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu318Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

17-4622695-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622695
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622695
    reference: chr 17
allele count: 1
allele frequency: 8.280613427842734e-6
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+111C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465877
  ensembl transcript: ENST00000571428
  gene symbol: ARRB2
  hgvsc: ENST00000571428.1:c.321C>G
  hgvsp: ENST00000571428.1:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.321C>G
  hgvsp: ENST00000574954.1:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.321C>G
  hgvsp: ENST00000572457.1:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.960C>G
  hgvsp: ENST00000412477.3:c.960C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.897C>G
  hgvsp: ENST00000269260.2:c.897C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.321C>G
  hgvsp: ENST00000571206.1:c.321C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*188C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000458371
  ensembl transcript: ENST00000574502
  gene symbol: ARRB2
  hgvsc: ENST00000574502.1:c.*375C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.852C>G
  hgvsp: ENST00000346341.2:c.852C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.852C>G
  hgvsp: ENST00000381488.6:c.852C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr320Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

17-4622700-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622700
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622700
    reference: chr 17
allele count: 3
allele frequency: 2.488965585902499e-5
allele num: 120532
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000458371
  ensembl transcript: ENST00000574502
  gene symbol: ARRB2
  hgvsc: ENST00000574502.1:c.*380T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+116T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.902T>G
  hgvsp: ENSP00000269260.2:p.Leu301Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.857T>G
  hgvsp: ENSP00000341895.2:p.Leu286Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.326T>G
  hgvsp: ENSP00000460607.1:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.326T>G
  hgvsp: ENSP00000466344.1:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.965T>G
  hgvsp: ENSP00000403701.3:p.Leu322Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.326T>G
  hgvsp: ENSP00000465296.1:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*193T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465877
  ensembl transcript: ENST00000571428
  gene symbol: ARRB2
  hgvsc: ENST00000571428.1:c.326T>G
  hgvsp: ENSP00000465877.1:p.Leu109Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.857T>G
  hgvsp: ENSP00000370898.6:p.Leu286Arg
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3180
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu322Arg
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

17-4622735-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622735
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622735
    reference: chr 17
allele count: 3
allele frequency: 2.548939641109299e-5
allele num: 117696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+20G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+20G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+20G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+20G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+20G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+151G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+20G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+20G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+20G>A
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8813
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18922
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 665
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3655
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

17-4622739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622739
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622739
    reference: chr 17
allele count: 1
allele frequency: 8.525439912699495e-6
allele num: 117296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+24C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+24C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+24C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+24C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+24C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+24C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+24C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+155C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+24C>T
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8759
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4459
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10678
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

17-4622745-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622745
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622745
    reference: chr 17
allele count: 39
allele frequency: 3.334245263661856e-4
allele num: 116968
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+30C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+30C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+30C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+30C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+30C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+30C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+30C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+161C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+30C>T
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7110
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1759
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9606
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8725
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10962
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 4.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4141
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3680
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/17-4622750-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622750
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622749
    reference: chr 17
allele count: 82
allele frequency: 7.021389550117309e-4
allele num: 116786
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+36delA
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+36delA
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+167delA
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+36delA
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+36delA
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+36delA
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+36delA
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+36delA
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+36delA
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8682
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9191
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7110
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5096
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3728
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: CA
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

17-4622761-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622761
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622761
    reference: chr 17
allele count: 6
allele frequency: 5.18887505188875e-5
allele num: 115632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+46C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+177C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+46C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+46C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+46C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+46C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+46C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+46C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+46C>T
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8451
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9524
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7101
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1367
  bin: 2.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

17-4622762-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622762
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622762
    reference: chr 17
allele count: 13
allele frequency: 1.125833549839785e-4
allele num: 115470
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+47G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+47G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+47G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+47G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+47G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+178G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+47G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+47G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+47G>A
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8402
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9250
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7046
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7436
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2038
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1384
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18872
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6325
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/17-4622764-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622764
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622764
    reference: chr 17
allele count: 1
allele frequency: 8.674682072902028e-6
allele num: 115278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+49C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+49C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+180C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+49C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+49C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+49C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+49C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+49C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+49C>A
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3637
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5825
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD

17-4622764-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622764
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622764
    reference: chr 17
allele count: 1
allele frequency: 8.674682072902028e-6
allele num: 115278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+49C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+49C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+180C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+49C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+49C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+49C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+49C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+49C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+49C>G
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2250
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4259
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3637
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

17-4622764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622764
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622764
    reference: chr 17
allele count: 2
allele frequency: 1.734936414580406e-5
allele num: 115278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+49C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+49C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+180C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+49C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+49C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+49C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+49C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+49C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+49C>T
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7038
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2945
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD

17-4622765-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4622765
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4622765
    reference: chr 17
allele count: 4
allele frequency: 3.469993233513194e-5
allele num: 115274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*208+50G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.341+50G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.980+50G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.341+50G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.917+50G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.786+181G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.341+50G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.872+50G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.872+50G>A
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7404
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3997
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8942
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8337
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4085
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

17-4623470-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623470
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623470
    reference: chr 17
allele count: 2
allele frequency: 4.105090311986864e-5
allele num: 48720
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.342-41G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.787-41G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.918-41G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.342-41G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*209-41G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.342-41G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.873-41G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.873-41G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.981-41G>T
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27199
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11425
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8655
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6833
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3385
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

17-4623479-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623479
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623479
    reference: chr 17
allele count: 10
allele frequency: 1.917986880969734e-4
allele num: 52138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.342-32C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.873-32C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.873-32C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.981-32C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.918-32C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.342-32C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*209-32C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.787-32C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.342-32C>T
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28164
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 5033
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4650
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 7.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

17-4623496-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623496
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623496
    reference: chr 17
allele count: 1
allele frequency: 1.578531965272297e-5
allele num: 63350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.787-15C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*209-15C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.873-15C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.342-15C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.918-15C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.342-15C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.342-15C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.981-15C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.873-15C>T
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3761
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

17-4623497-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623497
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623497
    reference: chr 17
allele count: 1
allele frequency: 1.544163063619518e-5
allele num: 64760
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.981-14A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.873-14A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*209-14A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.342-14A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.787-14A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.342-14A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.918-14A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.873-14A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.342-14A>G
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12932
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26542
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15778
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-4623504-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623504
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623504
    reference: chr 17
allele count: 2
allele frequency: 2.735454222173592e-5
allele num: 73114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.918-7A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.342-7A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*209-7A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.873-7A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.787-7A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.342-7A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.873-7A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.342-7A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.981-7A>G
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18113
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3025
  bin: 2.75e1
  variant carriers: 0
hgvs: c.981-7A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum

17-4623505-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623505
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623505
    reference: chr 17
allele count: 279
allele frequency: 3.766707168894289e-3
allele num: 74070
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.342-6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*209-6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.918-6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.787-6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.981-6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.873-6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.342-6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.342-6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.873-6T>C
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 7209
  bin: 1.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18622
  bin: 2.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 2.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 22467
  bin: 7.5e0
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.75e1
  variant carriers: 2
hgvs: c.981-6T>C
num of homozygotes: 6
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

17-4623507-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623507
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623507
    reference: chr 17
allele count: 1
allele frequency: 1.312749422390254e-5
allele num: 76176
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.342-4G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*209-4G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.873-4G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.981-4G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.342-4G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.787-4G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.873-4G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.342-4G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.918-4G>A
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6883
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2640
  bin: 6.75e1
  variant carriers: 0
hgvs: c.981-4G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

17-4623511-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623511
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623511
    reference: chr 17
allele count: 9
allele frequency: 1.091464745688714e-4
allele num: 82458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.873C>T
  hgvsp: ENST00000346341.2:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.342C>T
  hgvsp: ENST00000572457.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*209C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.787C>T
  hgvsp: ENSP00000466857.1:p.Arg263Cys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.873C>T
  hgvsp: ENST00000381488.6:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.981C>T
  hgvsp: ENST00000412477.3:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.342C>T
  hgvsp: ENST00000571206.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.918C>T
  hgvsp: ENST00000269260.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.342C>T
  hgvsp: ENST00000574954.1:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6494
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22930
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18434
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg263Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

17-4623512-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623512
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623512
    reference: chr 17
allele count: 41
allele frequency: 4.788936388908356e-4
allele num: 85614
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.982G>A
  hgvsp: ENSP00000403701.3:p.Val328Met
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.788G>A
  hgvsp: ENSP00000466857.1:p.Arg263His
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.343G>A
  hgvsp: ENSP00000466344.1:p.Val115Met
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.343G>A
  hgvsp: ENSP00000460607.1:p.Val115Met
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.874G>A
  hgvsp: ENSP00000370898.6:p.Val292Met
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.919G>A
  hgvsp: ENSP00000269260.2:p.Val307Met
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*210G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.343G>A
  hgvsp: ENSP00000465296.1:p.Val115Met
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.874G>A
  hgvsp: ENSP00000341895.2:p.Val292Met
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5396
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24520
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val328Met
num of homozygotes: 1
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

17-4623517-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623517
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623517
    reference: chr 17
allele count: 2
allele frequency: 2.105307480157477e-5
allele num: 94998
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.987G>A
  hgvsp: ENST00000412477.3:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.924G>A
  hgvsp: ENST00000269260.2:c.924G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.879G>A
  hgvsp: ENST00000381488.6:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.793G>A
  hgvsp: ENSP00000466857.1:p.Gly265Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.879G>A
  hgvsp: ENST00000346341.2:c.879G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*215G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.348G>A
  hgvsp: ENST00000572457.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.348G>A
  hgvsp: ENST00000574954.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.348G>A
  hgvsp: ENST00000571206.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30241
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1542
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly265Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

17-4623518-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623518
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623518
    reference: chr 17
allele count: 6
allele frequency: 6.215555463473253e-5
allele num: 96532
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.794G>C
  hgvsp: ENSP00000466857.1:p.Gly265Ala
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.988G>C
  hgvsp: ENSP00000403701.3:p.Glu330Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.349G>C
  hgvsp: ENSP00000466344.1:p.Glu117Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*216G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.349G>C
  hgvsp: ENSP00000460607.1:p.Glu117Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.925G>C
  hgvsp: ENSP00000269260.2:p.Glu309Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.349G>C
  hgvsp: ENSP00000465296.1:p.Glu117Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.880G>C
  hgvsp: ENSP00000370898.6:p.Glu294Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.880G>C
  hgvsp: ENSP00000341895.2:p.Glu294Gln
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3601
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11951
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31074
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34527
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu330Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

17-4623530-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623530
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623530
    reference: chr 17
allele count: 1
allele frequency: 9.128585251857668e-6
allele num: 109546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*228A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.361A>G
  hgvsp: ENSP00000460607.1:p.Lys121Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.892A>G
  hgvsp: ENSP00000341895.2:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.361A>G
  hgvsp: ENSP00000465296.1:p.Lys121Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.892A>G
  hgvsp: ENSP00000370898.6:p.Lys298Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.361A>G
  hgvsp: ENSP00000466344.1:p.Lys121Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.937A>G
  hgvsp: ENSP00000269260.2:p.Lys313Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.806A>G
  hgvsp: ENSP00000466857.1:p.Gln269Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1000A>G
  hgvsp: ENSP00000403701.3:p.Lys334Glu
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41292
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys334Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

17-4623555-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623555
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623555
    reference: chr 17
allele count: 2
allele frequency: 1.674116485025028e-5
allele num: 119466
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1025C>T
  hgvsp: ENSP00000403701.3:p.Ser342Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.831C>T
  hgvsp: ENST00000575877.1:c.831C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.386C>T
  hgvsp: ENSP00000466344.1:p.Ser129Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.386C>T
  hgvsp: ENSP00000460607.1:p.Ser129Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.386C>T
  hgvsp: ENSP00000465296.1:p.Ser129Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.917C>T
  hgvsp: ENSP00000341895.2:p.Ser306Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.962C>T
  hgvsp: ENSP00000269260.2:p.Ser321Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*253C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.917C>T
  hgvsp: ENSP00000370898.6:p.Ser306Phe
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser342Phe
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

17-4623565-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623565
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623565
    reference: chr 17
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.927C>G
  hgvsp: ENST00000381488.6:c.927C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.396C>G
  hgvsp: ENST00000571206.1:c.396C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*263C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1035C>G
  hgvsp: ENST00000412477.3:c.1035C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.841C>G
  hgvsp: ENSP00000466857.1:p.Gln281Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.396C>G
  hgvsp: ENST00000574954.1:c.396C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.972C>G
  hgvsp: ENST00000269260.2:c.972C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.927C>G
  hgvsp: ENST00000346341.2:c.927C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.396C>G
  hgvsp: ENST00000572457.1:c.396C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6232
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln281Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

17-4623580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623580
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623580
    reference: chr 17
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*278G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.942G>A
  hgvsp: ENST00000381488.6:c.942G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.987G>A
  hgvsp: ENST00000269260.2:c.987G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.411G>A
  hgvsp: ENST00000571206.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.411G>A
  hgvsp: ENST00000574954.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1050G>A
  hgvsp: ENST00000412477.3:c.1050G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.411G>A
  hgvsp: ENST00000572457.1:c.411G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.856G>A
  hgvsp: ENSP00000466857.1:p.Gly286Ser
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.942G>A
  hgvsp: ENST00000346341.2:c.942G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly286Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

17-4623583-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623583
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623583
    reference: chr 17
allele count: 16
allele frequency: 1.321877065432915e-4
allele num: 121040
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1053G>A
  hgvsp: ENST00000412477.3:c.1053G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.859G>A
  hgvsp: ENSP00000466857.1:p.Val287Ile
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.945G>A
  hgvsp: ENST00000381488.6:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.414G>A
  hgvsp: ENST00000574954.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*281G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.990G>A
  hgvsp: ENST00000269260.2:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.945G>A
  hgvsp: ENST00000346341.2:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.414G>A
  hgvsp: ENST00000571206.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.414G>A
  hgvsp: ENST00000572457.1:c.414G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val287Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD

17-4623592-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623592
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623592
    reference: chr 17
allele count: 1
allele frequency: 8.258729477057249e-6
allele num: 121084
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.423C>T
  hgvsp: ENST00000574954.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.423C>T
  hgvsp: ENST00000572457.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.999C>T
  hgvsp: ENST00000269260.2:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1062C>T
  hgvsp: ENST00000412477.3:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*290C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.954C>T
  hgvsp: ENST00000346341.2:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.423C>T
  hgvsp: ENST00000571206.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.868C>T
  hgvsp: ENSP00000466857.1:p.Arg290Trp
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.954C>T
  hgvsp: ENST00000381488.6:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14374
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg290Trp
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

17-4623594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623594
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623594
    reference: chr 17
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064G>A
  hgvsp: ENSP00000403701.3:p.Gly355Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425G>A
  hgvsp: ENSP00000466344.1:p.Gly142Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425G>A
  hgvsp: ENSP00000460607.1:p.Gly142Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870G>A
  hgvsp: ENST00000575877.1:c.870G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956G>A
  hgvsp: ENSP00000370898.6:p.Gly319Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956G>A
  hgvsp: ENSP00000341895.2:p.Gly319Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*292G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001G>A
  hgvsp: ENSP00000269260.2:p.Gly334Glu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425G>A
  hgvsp: ENSP00000465296.1:p.Gly142Glu
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly355Glu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD

17-4623596-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623596
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623596
    reference: chr 17
allele count: 326
allele frequency: 2.922089562941451e-3
allele num: 111564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+2T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+2T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*294T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+2T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+2T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+2T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+2T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+2T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+2T>G
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 13659
  bin: 2.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 4.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 3.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 28490
  bin: 2.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 3.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 5.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 4.25e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 8.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 3.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 7.5e0
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 1.25e1
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 2653
  bin: 2.5e0
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 3.25e1
  variant carriers: 21
hgvs: c.1064+2T>G
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

17-4623600-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623600
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623600
    reference: chr 17
allele count: 2
allele frequency: 1.651309488424321e-5
allele num: 121116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*298T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+6T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+6T>C
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 8.75e1
  variant carriers: 0
hgvs: c.1064+6T>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

17-4623605-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623605
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623604
    reference: chr 17
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+16delG
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+16delG
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+16delG
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*308delG
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+16delG
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+16delG
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+16delG
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+16delG
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+16delG
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3002
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2135
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: TG
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

17-4623611-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623611
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623611
    reference: chr 17
allele count: 9
allele frequency: 7.925604987847406e-5
allele num: 113556
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+17A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*309A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+17A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+17A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+17A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+17A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+17A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+17A>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+17A>G
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2736
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1685
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6202
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

17-4623612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623612
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623612
    reference: chr 17
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*310G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+18G>A
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

17-4623618-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623618
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623618
    reference: chr 17
allele count: 2
allele frequency: 1.648750247312537e-5
allele num: 121304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+24G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+24G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+24G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+24G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+24G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*316G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+24G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+24G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+24G>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18967
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44743
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

17-4623619-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623619
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623619
    reference: chr 17
allele count: 29
allele frequency: 2.407238316593343e-4
allele num: 120470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+25T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*317T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+25T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+25T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+25T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+25T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+25T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+25T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+25T>G
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27297
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18856
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8013
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44197
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1525
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

17-4623625-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623625
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623625
    reference: chr 17
allele count: 20
allele frequency: 1.656204971927326e-4
allele num: 120758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+31T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+31T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+31T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*323T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+31T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+31T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+31T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+31T>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+31T>G
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27269
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19405
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45025
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1927
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

17-4623633-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623633
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623633
    reference: chr 17
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+39G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+39G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+39G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+39G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+39G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+39G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*331G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+39G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+39G>C
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7668
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/17-4623636-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623636
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623636
    reference: chr 17
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+42C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+42C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+42C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+42C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+42C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+42C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+42C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*334C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+42C>A
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

17-4623636-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623636
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623636
    reference: chr 17
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.425+42C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1001+42C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.870+42C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.425+42C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.956+42C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1064+42C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.425+42C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.956+42C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*334C>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8317
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2014
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

17-4623645-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623645
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623645
    reference: chr 17
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-43C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-43C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-43C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*343C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-43C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-43C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-43C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-43C>G
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-43C>G
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2258
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45940
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1658
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1535
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

17-4623649-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623649
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623649
    reference: chr 17
allele count: 24
allele frequency: 1.977815502777183e-4
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-39T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-39T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-39T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-39T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*347T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-39T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-39T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-39T>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-39T>C
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 27336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

17-4623649-TGTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623649
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623646
    reference: chr 17
allele count: 295
allele frequency: 2.431064888830287e-3
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-32_1065-30delGTC
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*354_*356delGTC
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-32_426-30delGTC
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-32_871-30delGTC
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-32_426-30delGTC
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-32_957-30delGTC
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-32_426-30delGTC
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-32_957-30delGTC
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-32_1002-30delGTC
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 27336
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 8290
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 19878
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1883
  bin: 9.75e1
  variant carriers: 289
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 6
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: TGTC
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

17-4623652-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623652
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623652
    reference: chr 17
allele count: 19
allele frequency: 1.570144122702631e-4
allele num: 121008
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-36C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*350C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-36C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-36C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-36C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-36C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-36C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-36C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-36C>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 8286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 9.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

17-4623653-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623653
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623653
    reference: chr 17
allele count: 17
allele frequency: 1.40772759642934e-4
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-35G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-35G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-35G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-35G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-35G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*351G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-35G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-35G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-35G>A
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1512
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

17-4623655-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623655
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623655
    reference: chr 17
allele count: 3
allele frequency: 2.472350876036327e-5
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-33C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-33C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-33C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-33C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*353C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-33C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-33C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-33C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-33C>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

17-4623656-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623656
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623656
    reference: chr 17
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-32G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-32G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*354G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-32G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-32G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-32G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-32G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-32G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-32G>A
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1988
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

17-4623656-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623656
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623656
    reference: chr 17
allele count: 33
allele frequency: 2.71958596363996e-4
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-32G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-32G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-32G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-32G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*354G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-32G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-32G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-32G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-32G>C
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20004
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 9.75e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 7628
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

17-4623656-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623656
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623656
    reference: chr 17
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-32G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-32G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*354G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-32G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-32G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-32G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-32G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-32G>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-32G>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27379
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

17-4623666-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623666
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623666
    reference: chr 17
allele count: 1808
allele frequency: 1.490199957140267e-2
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-22C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-22C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-22C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-22C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*364C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-22C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-22C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-22C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-22C>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2139
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 834
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26834
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 4.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 19790
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 9.75e1
  variant carriers: 1260
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 27
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 160
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

17-4623667-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623667
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623667
    reference: chr 17
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-21G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-21G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-21G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-21G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-21G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-21G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*365G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-21G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-21G>A
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27052
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8566
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

17-4623670-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623670
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623670
    reference: chr 17
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*368G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-18G>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-18G>A
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46560
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7788
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum

17-4623672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623672
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623672
    reference: chr 17
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-16C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-16C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-16C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-16C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*370C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-16C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-16C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-16C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-16C>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46538
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/17-4623677-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623677
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623677
    reference: chr 17
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-11C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*375C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-11C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-11C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-11C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-11C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-11C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-11C>A
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-11C>A
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46592
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

17-4623677-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623677
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623677
    reference: chr 17
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*375C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-11C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-11C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-11C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-11C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-11C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-11C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-11C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-11C>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46592
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

17-4623679-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623679
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623679
    reference: chr 17
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*377C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-9C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-9C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-9C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-9C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-9C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-9C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-9C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-9C>T
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP

17-4623684-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623684
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623684
    reference: chr 17
allele count: 2
allele frequency: 1.648641519388024e-5
allele num: 121312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.957-4C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.871-4C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1065-4C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.957-4C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1002-4C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.426-4C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.426-4C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*382C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.426-4C>T
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: c.1065-4C>T
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

17-4623696-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623696
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623696
    reference: chr 17
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.965C>T
  hgvsp: ENSP00000370898.6:p.Ser322Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*394C>T
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.965C>T
  hgvsp: ENSP00000341895.2:p.Ser322Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1073C>T
  hgvsp: ENSP00000403701.3:p.Ser358Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1010C>T
  hgvsp: ENSP00000269260.2:p.Ser337Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.434C>T
  hgvsp: ENSP00000465296.1:p.Ser145Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.434C>T
  hgvsp: ENSP00000466344.1:p.Ser145Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.434C>T
  hgvsp: ENSP00000460607.1:p.Ser145Phe
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.879C>T
  hgvsp: ENST00000575877.1:c.879C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27131
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser358Phe
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

17-4623698-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623698
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623698
    reference: chr 17
allele count: 2
allele frequency: 1.649321304283287e-5
allele num: 121262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460879
  ensembl transcript: ENST00000576235
  gene symbol: ARRB2
  hgvsc: ENST00000576235.1:c.*396G>C
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.436G>C
  hgvsp: ENSP00000460607.1:p.Val146Leu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.436G>C
  hgvsp: ENSP00000465296.1:p.Val146Leu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1012G>C
  hgvsp: ENSP00000269260.2:p.Val338Leu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1075G>C
  hgvsp: ENSP00000403701.3:p.Val359Leu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.967G>C
  hgvsp: ENSP00000370898.6:p.Val323Leu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.881G>C
  hgvsp: ENSP00000466857.1:p.Cys294Ser
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.967G>C
  hgvsp: ENSP00000341895.2:p.Val323Leu
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.436G>C
  hgvsp: ENSP00000466344.1:p.Val146Leu
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val359Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/17-4623727-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623727
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623727
    reference: chr 17
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1041C>A
  hgvsp: ENST00000269260.2:c.1041C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1104C>A
  hgvsp: ENST00000412477.3:c.1104C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.910C>A
  hgvsp: ENSP00000466857.1:p.Gln304Lys
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.465C>A
  hgvsp: ENST00000572457.1:c.465C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.465C>A
  hgvsp: ENST00000571206.1:c.465C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.996C>A
  hgvsp: ENST00000381488.6:c.996C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.996C>A
  hgvsp: ENST00000346341.2:c.996C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.465C>A
  hgvsp: ENST00000574954.1:c.465C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8476
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7672
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln304Lys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

17-4623732-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623732
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623732
    reference: chr 17
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.1001C>G
  hgvsp: ENSP00000370898.6:p.Pro334Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1109C>G
  hgvsp: ENSP00000403701.3:p.Pro370Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.1001C>G
  hgvsp: ENSP00000341895.2:p.Pro334Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.470C>G
  hgvsp: ENSP00000466344.1:p.Pro157Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.470C>G
  hgvsp: ENSP00000465296.1:p.Pro157Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1046C>G
  hgvsp: ENSP00000269260.2:p.Pro349Arg
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.915C>G
  hgvsp: ENST00000575877.1:c.915C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.470C>G
  hgvsp: ENSP00000460607.1:p.Pro157Arg
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7649
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46190
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro370Arg
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

17-4623733-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623733
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623733
    reference: chr 17
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1110C>G
  hgvsp: ENST00000412477.3:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.471C>G
  hgvsp: ENST00000571206.1:c.471C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1047C>G
  hgvsp: ENST00000269260.2:c.1047C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.471C>G
  hgvsp: ENST00000574954.1:c.471C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.1002C>G
  hgvsp: ENST00000381488.6:c.1002C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.1002C>G
  hgvsp: ENST00000346341.2:c.1002C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.916C>G
  hgvsp: ENSP00000466857.1:p.Pro306Ala
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.471C>G
  hgvsp: ENST00000572457.1:c.471C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46224
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro306Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

17-4623736-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623736
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623736
    reference: chr 17
allele count: 2
allele frequency: 1.658897496723677e-5
allele num: 120562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1050C>G
  hgvsp: ENSP00000269260.2:p.His350Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.474C>G
  hgvsp: ENSP00000465296.1:p.His158Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.474C>G
  hgvsp: ENSP00000460607.1:p.His158Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.1005C>G
  hgvsp: ENSP00000370898.6:p.His335Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.919C>G
  hgvsp: ENSP00000466857.1:p.Arg307Gly
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.474C>G
  hgvsp: ENSP00000466344.1:p.His158Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1113C>G
  hgvsp: ENSP00000403701.3:p.His371Gln
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.1005C>G
  hgvsp: ENSP00000341895.2:p.His335Gln
  variant of: http://identifiers.org/hgnc/712
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1899
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His371Gln
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

17-4623736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4623736
    reference: chr 17
  end: Position
    type: ExactPosition
    position: 4623736
    reference: chr 17
allele count: 3
allele frequency: 2.488346245085516e-5
allele num: 120562
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000403701
  ensembl transcript: ENST00000412477
  gene symbol: ARRB2
  hgvsc: ENST00000412477.3:c.1113C>T
  hgvsp: ENST00000412477.3:c.1113C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466857
  ensembl transcript: ENST00000575877
  gene symbol: ARRB2
  hgvsc: ENST00000575877.1:c.919C>T
  hgvsp: ENSP00000466857.1:p.Arg307Ter
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000269260
  ensembl transcript: ENST00000269260
  gene symbol: ARRB2
  hgvsc: ENST00000269260.2:c.1050C>T
  hgvsp: ENST00000269260.2:c.1050C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000341895
  ensembl transcript: ENST00000346341
  gene symbol: ARRB2
  hgvsc: ENST00000346341.2:c.1005C>T
  hgvsp: ENST00000346341.2:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000466344
  ensembl transcript: ENST00000574954
  gene symbol: ARRB2
  hgvsc: ENST00000574954.1:c.474C>T
  hgvsp: ENST00000574954.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000465296
  ensembl transcript: ENST00000572457
  gene symbol: ARRB2
  hgvsc: ENST00000572457.1:c.474C>T
  hgvsp: ENST00000572457.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000460607
  ensembl transcript: ENST00000571206
  gene symbol: ARRB2
  hgvsc: ENST00000571206.1:c.474C>T
  hgvsp: ENST00000571206.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000141480
  ensembl protein: ENSP00000370898
  ensembl transcript: ENST00000381488
  gene symbol: ARRB2
  hgvsc: ENST00000381488.6:c.1005C>T
  hgvsp: ENST00000381488.6:c.1005C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/712
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26793
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg307Ter
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 7284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19011
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 212
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4800
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3710
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4319
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16357
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2297
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

FS
type: SiteQuality
SIO_000300: 4.662e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.51e0

QD
type: SiteQuality
SIO_000300: 1.299e1

MQRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.266495e6

VQSLOD
type: SiteQuality
SIO_000300: 8.31e-1

GenotypeDepth
all individuals: 214
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2998
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16207
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2297
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3708
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4309
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6797
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19010
bin: 9.75e1
variant carriers: 2

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005168890491646e-5
allele num: 66552
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.595e0

VQSLOD
type: SiteQuality
SIO_000300: 3.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.636e0

MQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

QD
type: SiteQuality
SIO_000300: 9.33e0

DP
type: SiteQuality
SIO_000300: 2.263651e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeDepth
all individuals: 92
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2989
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16157
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6776
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4776
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19005
bin: 9.75e1
variant carriers: 49

GenotypeQuality
all individuals: 3706
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2296
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4303
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.093102607847916e-5
allele num: 16412
num of homozygotes: 0

East Asian
type: Population
allele count: 47
allele frequency: 5.441074322759898e-3
allele num: 8638
num of homozygotes: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.021e1

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.51e-2

DP
type: SiteQuality
SIO_000300: 2.262137e6

GenotypeDepth
all individuals: 194
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4786
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 415
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3707
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18963
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 16133
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4304
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 84
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2297
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6763
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2993
bin: 7.25e1
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: 1
allele frequency: 9.654373431164318e-5
allele num: 10358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66516
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: 3.16e-1

QD
type: SiteQuality
SIO_000300: 1.074e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.258725e6

FS
type: SiteQuality
SIO_000300: 5.928e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.629e0

GenotypeDepth
all individuals: 390
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4779
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18961
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16103
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6756
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2295
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4301
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3705
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2993
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503804625703029e-5
allele num: 66498
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

DP
type: SiteQuality
SIO_000300: 2.257207e6

VQSLOD
type: SiteQuality
SIO_000300: 2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.605e0

QD
type: SiteQuality
SIO_000300: 1.104e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 13183
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15747
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4287
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3699
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4753
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2973
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6687
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2295
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18956
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66434
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16312
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.686168151879117e-5
allele num: 10324
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e-1

DP
type: SiteQuality
SIO_000300: 2.250051e6

MQRankSum
type: SiteQuality
SIO_000300: -8.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 3.343e0

QD
type: SiteQuality
SIO_000300: 1.226e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.811e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeDepth
all individuals: 9269
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2955
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18954
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 199
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6617
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15436
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2288
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4276
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4741
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.522158577027435e-5
allele num: 66340
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.241879e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

FS
type: SiteQuality
SIO_000300: 5.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.59e0

VQSLOD
type: SiteQuality
SIO_000300: -8.879e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.256e1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-1

GenotypeQuality
all individuals: 2259
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11265
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4182
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4506
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5537
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.062787136294027e-5
allele num: 65300
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.713837574067619e-5
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15262
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.009e0

VQSLOD
type: SiteQuality
SIO_000300: 4.67e0

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

QD
type: SiteQuality
SIO_000300: 1.366e1

DP
type: SiteQuality
SIO_000300: 2.145489e6

GenotypeQuality
all individuals: 3507
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 767
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1337
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18904
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 276
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5414
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2683
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15074
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65174
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.039068994181214e-4
allele num: 9624
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.132349e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 2.497e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 1.123e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.106e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 2248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5316
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
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variant carriers: 0

GenotypeQuality
all individuals: 370
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 225
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variant carriers: 0

GenotypeQuality
all individuals: 1205
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variant carriers: 0

GenotypeQuality
all individuals: 136
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variant carriers: 0

GenotypeQuality
all individuals: 18897
bin: 9.75e1
variant carriers: 39

GenotypeQuality
all individuals: 10691
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2631
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 34
allele frequency: 5.22546337564934e-4
allele num: 65066
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.087246921310791e-4
allele num: 9582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14916
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.585753592173647e-4
allele num: 6542
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.314e1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

DP
type: SiteQuality
SIO_000300: 2.122494e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e-1

FS
type: SiteQuality
SIO_000300: 3.893e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.805e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

GenotypeQuality
all individuals: 2253
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 195
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10034
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 205
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variant carriers: 0

GenotypeQuality
all individuals: 1292
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18944
bin: 9.75e1
variant carriers: 79

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

African
type: Population
allele count: 68
allele frequency: 7.107023411371237e-3
allele num: 9568
num of homozygotes: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.747638326585695e-5
allele num: 14820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.075882009166129e-5
allele num: 65022
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 9.605309116311561e-4
allele num: 11452
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

QD
type: SiteQuality
SIO_000300: 1.569e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.022e1

VQSLOD
type: SiteQuality
SIO_000300: 6.5e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e0

DP
type: SiteQuality
SIO_000300: 2.109673e6

GenotypeQuality
all individuals: 263
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
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variant carriers: 0

GenotypeQuality
all individuals: 521
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variant carriers: 0

GenotypeQuality
all individuals: 3182
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2436
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variant carriers: 0

GenotypeQuality
all individuals: 4278
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1756
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18870
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4088
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3639
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.730364873222017e-5
allele num: 64680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.180358829084042e-4
allele num: 8472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14210
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.97e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

FS
type: SiteQuality
SIO_000300: 2.054e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

DP
type: SiteQuality
SIO_000300: 2.071093e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 1763
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
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GenotypeQuality
all individuals: 726
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variant carriers: 0

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

GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 1975
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1363
bin: 5.25e1
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GenotypeQuality
all individuals: 4082
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GenotypeQuality
all individuals: 2424
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4331
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.063144511936714e-5
allele num: 14158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.192525621574759e-5
allele num: 64594
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.748906386701662e-5
allele num: 11430
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.181474480151229e-4
allele num: 8464
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.351894982002964e-4
allele num: 9446
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 3.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.422e0

DP
type: SiteQuality
SIO_000300: 2.065847e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

GenotypeQuality
all individuals: 831
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4078
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4257
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 18861
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 521
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variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2945
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1375
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1741
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.102272727272727e-5
allele num: 14080
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9420
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.17e-1

FS
type: SiteQuality
SIO_000300: 6.983e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.08e-1

DP
type: SiteQuality
SIO_000300: 2.062081e6

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

GenotypeQuality
all individuals: 401
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2945
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 559
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GenotypeQuality
all individuals: 1375
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4257
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1741
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4078
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18861
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1973
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5825
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9420
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14080
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.550099206349206e-5
allele num: 64512
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.983e0

QD
type: SiteQuality
SIO_000300: 1.24e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.08e-1

DP
type: SiteQuality
SIO_000300: 2.062081e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e0

GenotypeQuality
all individuals: 2250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3637
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 831
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4078
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4259
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 2.5e0
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GenotypeQuality
all individuals: 1741
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5825
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1973
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4257
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.100198412698413e-5
allele num: 64512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14080
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.17e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

FS
type: SiteQuality
SIO_000300: 6.983e0

DP
type: SiteQuality
SIO_000300: 2.062081e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e0

QD
type: SiteQuality
SIO_000300: 1.24e1

VQSLOD
type: SiteQuality
SIO_000300: 5.08e-1

GenotypeQuality
all individuals: 1726
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1878
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6018
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1366
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4198
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18859
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variant carriers: 5

GenotypeQuality
all individuals: 4248
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3638
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14068
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.201935003721161e-5
allele num: 64496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9438
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

FS
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

DP
type: SiteQuality
SIO_000300: 2.060962e6

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.24e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

GenotypeQuality
all individuals: 484
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3043
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4702
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6751
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 518
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variant carriers: 0

GenotypeQuality
all individuals: 4506
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1806
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10856
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.152823920265781e-4
allele num: 4816
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.153e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.818e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 4.029e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.51e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.47271e5

GenotypeQuality
all individuals: 7844
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25588
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
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variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4873
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11040
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2764
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.212389380530973e-3
allele num: 452
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 3.054989816700611e-3
allele num: 2946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2034
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.226e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

DP
type: SiteQuality
SIO_000300: 7.87656e5

QD
type: SiteQuality
SIO_000300: 1.102e1

GenotypeQuality
all individuals: 167
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26819
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 565
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variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3695
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15110
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.89452356142179e-5
allele num: 34548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11742
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3854
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.277e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

QD
type: SiteQuality
SIO_000300: 3.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.342e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.19474e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.342e0

GenotypeQuality
all individuals: 406
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1631
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2194
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1427
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 616
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variant carriers: 0

GenotypeQuality
all individuals: 3581
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3696
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.63826998689384e-4
allele num: 6104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4016
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4236
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 9.2987e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.341e1

FS
type: SiteQuality
SIO_000300: 3.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.059e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
all individuals: 620
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2798
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20748
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 7.5e0
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GenotypeQuality
all individuals: 2531
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.972650422675286e-5
allele num: 40220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4832
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3172
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 578
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.42e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.012487e6

QD
type: SiteQuality
SIO_000300: 1.337e1

FS
type: SiteQuality
SIO_000300: 1.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.87e0

GenotypeQuality
all individuals: 701
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 215
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 22748
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 188
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 2955
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 346
bin: 8.25e1
variant carriers: 3

GenotypeQuality
all individuals: 857
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1469
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 491
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 21046
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1405
bin: 9.75e1
variant carriers: 255

GenotypeQuality
all individuals: 183
bin: 8.75e1
variant carriers: 6

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.38407009943881e-5
allele num: 40628
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.208727739451307e-4
allele num: 12466
num of homozygotes: 0

Latino
type: Population
allele count: 21
allele frequency: 3.942921517085993e-3
allele num: 5326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3210
num of homozygotes: 0

African
type: Population
allele count: 249
allele frequency: 3.600347021399653e-2
allele num: 6916
num of homozygotes: 6

Other
type: Population
allele count: 2
allele frequency: 3.367003367003367e-3
allele num: 594
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

DP
type: SiteQuality
SIO_000300: 1.025704e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

QD
type: SiteQuality
SIO_000300: 1.49e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

GenotypeQuality
all individuals: 1198
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 178
bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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bin: 7.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.388687177527231e-5
allele num: 41864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5102
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7104
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12616
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.843e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

QD
type: SiteQuality
SIO_000300: 1.28e1

DP
type: SiteQuality
SIO_000300: 1.045095e6

VQSLOD
type: SiteQuality
SIO_000300: -1.364e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeQuality
all individuals: 1208
bin: 9.75e1
variant carriers: 9

GenotypeQuality
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bin: 9.25e1
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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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
all individuals: 1365
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 1.42602495543672e-3
allele num: 5610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3626
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.642922653622745e-5
allele num: 13084
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45602
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 1.108142e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.141e0

VQSLOD
type: SiteQuality
SIO_000300: 8.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

QD
type: SiteQuality
SIO_000300: 9.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

FS
type: SiteQuality
SIO_000300: 8.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

GenotypeQuality
all individuals: 1310
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 39

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 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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variant carriers: 0

GenotypeQuality
all individuals: 670
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GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 2.959455460195324e-4
allele num: 6758
num of homozygotes: 0

East Asian
type: Population
allele count: 37
allele frequency: 6.237356709372893e-3
allele num: 5932
num of homozygotes: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.217807583618035e-5
allele num: 47418
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.88e0

FS
type: SiteQuality
SIO_000300: 1.575e0

DP
type: SiteQuality
SIO_000300: 1.136311e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.9e-2

QD
type: SiteQuality
SIO_000300: 1.219e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.6e-2

GenotypeQuality
all individuals: 941
bin: 7.25e1
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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GenotypeQuality
all individuals: 1207
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 427
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.249687578105474e-4
allele num: 8002
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4298
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.482359916987845e-4
allele num: 6746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52946
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.736e0

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.18e-1

DP
type: SiteQuality
SIO_000300: 1.224025e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

QD
type: SiteQuality
SIO_000300: 1.474e1

GenotypeQuality
all individuals: 1434
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 225
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GenotypeQuality
all individuals: 3690
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8254
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 8.73871249635887e-4
allele num: 6866
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14108
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.238274e6

FS
type: SiteQuality
SIO_000300: 8.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

QD
type: SiteQuality
SIO_000300: 1.162e1

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6107
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1221
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variant carriers: 1

GenotypeQuality
all individuals: 1197
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.639021831770799e-5
allele num: 61012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9948
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8004
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15282
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.63e-1

QD
type: SiteQuality
SIO_000300: 1.589e1

FS
type: SiteQuality
SIO_000300: 6.194e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.975e0

MQRankSum
type: SiteQuality
SIO_000300: -8.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.12e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 3.76e-1

DP
type: SiteQuality
SIO_000300: 1.370933e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1269
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 46327
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6194
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.767408978437611e-4
allele num: 11316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.348e1

VQSLOD
type: SiteQuality
SIO_000300: -3.699e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

FS
type: SiteQuality
SIO_000300: 4.792e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.926e0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.221e0

DP
type: SiteQuality
SIO_000300: 1.490385e6

MQ
type: SiteQuality
SIO_000300: 5.803e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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
all individuals: 550
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 83
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GenotypeQuality
all individuals: 376
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 1.506263e6

VQSLOD
type: SiteQuality
SIO_000300: -3.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.24e-1

FS
type: SiteQuality
SIO_000300: 5.098e0

QD
type: SiteQuality
SIO_000300: 1.127e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.599e0

GenotypeQuality
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bin: 4.25e1
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: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66552
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.029e0

VQSLOD
type: SiteQuality
SIO_000300: -1.038e0

MQ
type: SiteQuality
SIO_000300: 5.733e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.494e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.594e1

MQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.51762e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

South Asian
type: Population
allele count: 16
allele frequency: 9.704027171276079e-4
allele num: 16488
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
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: 1.093e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.196e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.519334e6

FS
type: SiteQuality
SIO_000300: 1.124e0

VQSLOD
type: SiteQuality
SIO_000300: 9.75e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
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: 16492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e0

VQSLOD
type: SiteQuality
SIO_000300: -1.124e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 8.316000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.919e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.531879e6

MQRankSum
type: SiteQuality
SIO_000300: -9.87e-1

QD
type: SiteQuality
SIO_000300: 1.029e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

GenotypeQuality
all individuals: 81
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1024
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GenotypeQuality
all individuals: 1848
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.531995e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 5.35e-1

FS
type: SiteQuality
SIO_000300: 4.606e0

MQRankSum
type: SiteQuality
SIO_000300: -3.73e-1

QD
type: SiteQuality
SIO_000300: 1.587e1

GenotypeQuality
all individuals: 1030
bin: 2.25e1
variant carriers: 32

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 27

GenotypeQuality
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GenotypeQuality
all individuals: 230
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variant carriers: 13

South Asian
type: Population
allele count: 9
allele frequency: 5.624296962879641e-4
allele num: 16002
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.032844453625284e-3
allele num: 9682
num of homozygotes: 0

East Asian
type: Population
allele count: 33
allele frequency: 4.158266129032258e-3
allele num: 7936
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 165
allele frequency: 3.024193548387097e-2
allele num: 5456
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.937233630375823e-3
allele num: 10324
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.694581280788177e-3
allele num: 812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 86
allele frequency: 1.401747294301734e-3
allele num: 61352
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.451e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.514e0

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

MQ
type: SiteQuality
SIO_000300: 5.928e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

QD
type: SiteQuality
SIO_000300: 6.6e-1

FS
type: SiteQuality
SIO_000300: 8.6185e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 1.714336e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

GenotypeQuality
all individuals: 100
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
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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: 126
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501456412720339e-5
allele num: 66602
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.819e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-1

QD
type: SiteQuality
SIO_000300: 9.83e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.057e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.887e-1

DP
type: SiteQuality
SIO_000300: 1.651499e6

GenotypeQuality
all individuals: 200
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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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 908
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MQRankSum
type: SiteQuality
SIO_000300: 8.0e-1

QD
type: SiteQuality
SIO_000300: 1.087e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.655754e6

MQ
type: SiteQuality
SIO_000300: 5.91e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.78e0

GenotypeQuality
all individuals: 334
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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
all individuals: 300
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 487
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variant carriers: 2

GenotypeQuality
all individuals: 1331
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.675715530531537e-5
allele num: 59676
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.170686022008897e-4
allele num: 8542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.674922600619196e-5
allele num: 10336
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.627727856225931e-4
allele num: 6232
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.511e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.44e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

QD
type: SiteQuality
SIO_000300: 2.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

FS
type: SiteQuality
SIO_000300: 4.6816e1

DP
type: SiteQuality
SIO_000300: 1.77082e6

VQSLOD
type: SiteQuality
SIO_000300: -1.174e1

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

GenotypeQuality
all individuals: 2085
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2273
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7491
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 483
bin: 9.25e1
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: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 3.005e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.764e0

QD
type: SiteQuality
SIO_000300: 1.103e1

DP
type: SiteQuality
SIO_000300: 1.646724e6

GenotypeQuality
all individuals: 1699
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2260
bin: 9.75e1
variant carriers: 2

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

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

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

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
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GenotypeQuality
all individuals: 482
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GenotypeQuality
all individuals: 2080
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7524
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.923446816695518e-4
allele num: 10398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 1.646927e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 1.591e0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.39e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.36e-1

GenotypeQuality
all individuals: 242
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1929
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 360
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 379
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variant carriers: 1

GenotypeQuality
all individuals: 66
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variant carriers: 2

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 7234
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 398
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 444
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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 809
bin: 8.25e1
variant carriers: 4

GenotypeQuality
all individuals: 1692
bin: 9.75e1
variant carriers: 7

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.524068041983351e-5
allele num: 66312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 25
allele frequency: 4.010266281681104e-3
allele num: 6234
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.05e1

QD
type: SiteQuality
SIO_000300: 5.0e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.46e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.948e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -5.462e0

MQRankSum
type: SiteQuality
SIO_000300: -1.57e-1

DP
type: SiteQuality
SIO_000300: 1.659043e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.47e-1

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 272
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
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variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 789
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variant carriers: 3

GenotypeQuality
all individuals: 173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
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variant carriers: 7

GenotypeQuality
all individuals: 7400
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variant carriers: 1

GenotypeQuality
all individuals: 294
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variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 17
allele frequency: 2.713054580274497e-3
allele num: 6266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007518796992481e-5
allele num: 66500
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

QD
type: SiteQuality
SIO_000300: 7.3e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.995e0

DP
type: SiteQuality
SIO_000300: 1.649957e6

FS
type: SiteQuality
SIO_000300: 2.7565e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.939e0

VQSLOD
type: SiteQuality
SIO_000300: -4.898e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 380
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1662
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variant carriers: 1

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 37
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 2023
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variant carriers: 0

GenotypeQuality
all individuals: 45923
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variant carriers: 0

GenotypeQuality
all individuals: 31
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GenotypeQuality
all individuals: 817
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 7.75e1
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: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.247e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.924e1

MQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.35e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e0

VQSLOD
type: SiteQuality
SIO_000300: 4.12e-1

DP
type: SiteQuality
SIO_000300: 1.634872e6

QD
type: SiteQuality
SIO_000300: 1.177e1

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

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2014
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 806
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 376
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variant carriers: 0

GenotypeQuality
all individuals: 7667
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1661
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 5.25e1
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: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.677e0

QD
type: SiteQuality
SIO_000300: 1.656e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

DP
type: SiteQuality
SIO_000300: 1.635018e6

MQRankSum
type: SiteQuality
SIO_000300: -1.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

FS
type: SiteQuality
SIO_000300: 3.939e0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7667
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1661
bin: 9.75e1
variant carriers: 2

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
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: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
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: 1.656e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.677e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 3.939e0

VQSLOD
type: SiteQuality
SIO_000300: 4.77e-1

DP
type: SiteQuality
SIO_000300: 1.635018e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

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

GenotypeQuality
all individuals: 7621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 5.75e1
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GenotypeQuality
all individuals: 69
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GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
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GenotypeQuality
all individuals: 361
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variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
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: 10398
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
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: 66676
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.635007e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.075e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.347e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 1883
bin: 9.75e1
variant carriers: 24

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7599
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variant carriers: 0

GenotypeQuality
all individuals: 793
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variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
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variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 24
allele frequency: 2.773284030506125e-3
allele num: 8654
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.762e1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 1.793e1

VQSLOD
type: SiteQuality
SIO_000300: 6.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.82e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

DP
type: SiteQuality
SIO_000300: 1.650552e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

GenotypeQuality
all individuals: 1511
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7599
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45886
bin: 6.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 21
allele frequency: 1.813784764207981e-3
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499100179964007e-5
allele num: 66680
num of homozygotes: 0

African
type: Population
allele count: 265
allele frequency: 2.547097270280661e-2
allele num: 10404
num of homozygotes: 6

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

South Asian
type: Population
allele count: 4
allele frequency: 2.42306760358614e-4
allele num: 16508
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.202643171806168e-3
allele num: 908
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.82e-2

QD
type: SiteQuality
SIO_000300: 1.793e1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.12e0

DP
type: SiteQuality
SIO_000300: 1.650552e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.95e-1

MQ
type: SiteQuality
SIO_000300: 5.762e1

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

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45878
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7587
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variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.893153937475267e-5
allele num: 10108
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.596053997923157e-4
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.649917504124794e-4
allele num: 66670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 4
allele frequency: 2.423948612289419e-4
allele num: 16502
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: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.634403e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.739e0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.98e-1

QD
type: SiteQuality
SIO_000300: 1.32e1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

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

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 1983
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variant carriers: 0

GenotypeQuality
all individuals: 7599
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variant carriers: 0

GenotypeQuality
all individuals: 1581
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45906
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 1.011531458628363e-4
allele num: 9886
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.600554785020804e-4
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049821530339842e-4
allele num: 66678
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 6.933210076265311e-4
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

FS
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

DP
type: SiteQuality
SIO_000300: 1.652042e6

QD
type: SiteQuality
SIO_000300: 1.274e1

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

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7633
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46072
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 1520
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999310158663508e-5
allele num: 66682
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

DP
type: SiteQuality
SIO_000300: 1.632851e6

FS
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.882e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.781e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.77e-1

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 7628
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46092
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 360
bin: 8.75e1
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: 1.499700059988002e-5
allele num: 66680
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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.634505e6

QD
type: SiteQuality
SIO_000300: 1.446e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.134e0

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

GenotypeQuality
all individuals: 793
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 360
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1988
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1518
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46092
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 17
allele frequency: 1.030178160223003e-3
allele num: 16502
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: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
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: 11
allele frequency: 1.649670065986803e-4
allele num: 66680
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

QD
type: SiteQuality
SIO_000300: 1.446e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.134e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

DP
type: SiteQuality
SIO_000300: 1.634505e6

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7628
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46092
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
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GenotypeQuality
all individuals: 1518
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1988
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variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 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: 8654
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
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: 1.134e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.9e0

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

DP
type: SiteQuality
SIO_000300: 1.634505e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.446e1

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7456
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
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GenotypeQuality
all individuals: 1432
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1911
bin: 7.25e1
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 53
bin: 4.75e1
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GenotypeQuality
all individuals: 2704
bin: 9.75e1
variant carriers: 1645

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45498
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 1

South Asian
type: Population
allele count: 5
allele frequency: 3.031772980839195e-4
allele num: 16492
num of homozygotes: 0

Latino
type: Population
allele count: 65
allele frequency: 5.614095698738988e-3
allele num: 11578
num of homozygotes: 2

African
type: Population
allele count: 1718
allele frequency: 1.651287966166859e-1
allele num: 10404
num of homozygotes: 158

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

Other
type: Population
allele count: 6
allele frequency: 6.622516556291391e-3
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.099643060679685e-4
allele num: 66678
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.485e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.4e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.787923e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.37e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.552e1

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 46538
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.23e-1

ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 4.04e-1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.27e-1

DP
type: SiteQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
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
allele num: 10402
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

InbreedingCoeff
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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SIO_000300: -3.0e-1

MQ
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SIO_000300: 5.932e1

FS
type: SiteQuality
SIO_000300: 6.98e-1

DP
type: SiteQuality
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MQRankSum
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SIO_000300: -1.645e0

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 frequency: 0.0e0
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num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
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)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.917e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.372e-1

FS
type: SiteQuality
SIO_000300: 8.720000000000001e0

DP
type: SiteQuality
SIO_000300: 1.614757e6

QD
type: SiteQuality
SIO_000300: 1.132e1

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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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 6.77e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.957e1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.18e-1

FS
type: SiteQuality
SIO_000300: 7.126e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.462e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 1.614553e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.77e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.957e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 7.126e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.462e0

ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.614553e6

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: 9.75e1
variant carriers: 1

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
allele num: 10402
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele frequency: 6.06060606060606e-5
allele num: 16500
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Other
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
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BaseQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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 frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

South Asian
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Latino
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African
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DP
type: SiteQuality
SIO_000300: 1.614459e6

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

European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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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
allele num: 8652
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 1.573e1

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

FS
type: SiteQuality
SIO_000300: 5.387e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -1.219e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.29e0

DP
type: SiteQuality
SIO_000300: 1.613923e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.96e-1

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 8622
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.196e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.606519e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.228e0

FS
type: SiteQuality
SIO_000300: 6.99e-1

QD
type: SiteQuality
SIO_000300: 1.287e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16316
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505661286437003e-5
allele num: 66416
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.154e0

QD
type: SiteQuality
SIO_000300: 1.089e1

DP
type: SiteQuality
SIO_000300: 1.603427e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 1.4482e1

VQSLOD
type: SiteQuality
SIO_000300: -1.229e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.227e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.655011251514626e-5
allele num: 11554
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16318
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.244e0

FS
type: SiteQuality
SIO_000300: 1.1597e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.603462e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 5.934e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.66e-1

QD
type: SiteQuality
SIO_000300: 9.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.152e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 6.75e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.01504507492387e-5
allele num: 66334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
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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: 900
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

QD
type: SiteQuality
SIO_000300: 1.177e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.66e-1

FS
type: SiteQuality
SIO_000300: 5.075e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e-1

VQSLOD
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SIO_000300: 1.28e0

DP
type: SiteQuality
SIO_000300: 1.601658e6