18-32650298-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32650298
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32650298
    reference: chr 18
allele count: 3
allele frequency: 2.547121752419766e-5
allele num: 117780
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166974
  ensembl transcript: ENST00000585592
  gene symbol: MAPRE2
  hgvsc: ENST00000585592.1:n.312T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.121+12T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.17+64T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.121+12T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.121+12T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-27112T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.250+12T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.121+12T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.121+12T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.250+12T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.214+12T>G
  variant of: http://identifiers.org/hgnc/6891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS

18-32650302-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32650302
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32650302
    reference: chr 18
allele count: 3
allele frequency: 2.542415973152087e-5
allele num: 117998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166974
  ensembl transcript: ENST00000585592
  gene symbol: MAPRE2
  hgvsc: ENST00000585592.1:n.316T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.121+16T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.17+68T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.121+16T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-27108T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.214+16T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.121+16T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.250+16T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.250+16T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.121+16T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.121+16T>G
  variant of: http://identifiers.org/hgnc/6891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4890
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7983
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

18-32650312-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32650312
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32650312
    reference: chr 18
allele count: 3
allele frequency: 2.553148031522868e-5
allele num: 117502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.214+26A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.121+26A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.121+26A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.121+26A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.17+78A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.121+26A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.250+26A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166974
  ensembl transcript: ENST00000585592
  gene symbol: MAPRE2
  hgvsc: ENST00000585592.1:n.326A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.250+26A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.121+26A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-27098A>G
  variant of: http://identifiers.org/hgnc/6891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3224
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7957
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4370
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

18-32650327-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32650327
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32650327
    reference: chr 18
allele count: 35
allele frequency: 3.009924149911422e-4
allele num: 116282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.121+41G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.250+41G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.121+41G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.121+41G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.121+41G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166974
  ensembl transcript: ENST00000585592
  gene symbol: MAPRE2
  hgvsc: ENST00000585592.1:n.341G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.214+41G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.17+93G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.250+41G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.121+41G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-27083G>C
  variant of: http://identifiers.org/hgnc/6891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12081
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11061
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 721
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

18-32650329-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32650329
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32650329
    reference: chr 18
allele count: 1
allele frequency: 8.614154779133072e-6
allele num: 116088
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.250+43C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.121+43C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.121+43C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.214+43C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.121+43C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166974
  ensembl transcript: ENST00000585592
  gene symbol: MAPRE2
  hgvsc: ENST00000585592.1:n.343C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.250+43C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.121+43C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.121+43C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-27081C>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.17+95C>G
  variant of: http://identifiers.org/hgnc/6891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7912
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2817
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3006
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/18-32650334-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32650334
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32650334
    reference: chr 18
allele count: 1
allele frequency: 8.643789437289307e-6
allele num: 115690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.17+100A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.250+48A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-27076A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166974
  ensembl transcript: ENST00000585592
  gene symbol: MAPRE2
  hgvsc: ENST00000585592.1:n.348A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.250+48A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.214+48A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.121+48A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.121+48A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.121+48A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.121+48A>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.121+48A>C
  variant of: http://identifiers.org/hgnc/6891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 3.25e1
  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: A
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

18-32650335-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32650335
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32650335
    reference: chr 18
allele count: 17
allele frequency: 1.469571230982019e-4
allele num: 115680
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.121+49T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.250+49T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.214+49T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-27075T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.121+49T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.17+101T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.121+49T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.250+49T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.121+49T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166974
  ensembl transcript: ENST00000585592
  gene symbol: MAPRE2
  hgvsc: ENST00000585592.1:n.349T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.121+49T>C
  variant of: http://identifiers.org/hgnc/6891
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7855
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4874
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10967
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 3.25e1
  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: T
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-32677369-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677369
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677369
    reference: chr 18
allele count: 1
allele frequency: 8.531112968997936e-6
allele num: 117218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.215-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.122-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.122-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.251-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.122-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.251-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.122-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.122-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-41A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-90A>G
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6941
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39606
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/18-32677380-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677380
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677380
    reference: chr 18
allele count: 2
allele frequency: 1.704245274979975e-5
allele num: 117354
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.251-30C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.122-30C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.122-30C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.215-30C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.122-30C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-30C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.122-30C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-79C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.122-30C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.251-30C>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6954
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 994
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-32677380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677380
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677380
    reference: chr 18
allele count: 1
allele frequency: 8.521226374899876e-6
allele num: 117354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.251-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.122-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.215-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.122-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.251-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.122-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.122-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.122-30C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-79C>T
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29280
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2090
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1809
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS

18-32677387-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677387
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677387
    reference: chr 18
allele count: 1
allele frequency: 8.494733265375467e-6
allele num: 117720
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.122-23G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-23G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-72G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.122-23G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.122-23G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.251-23G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.122-23G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.215-23G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.122-23G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.251-23G>C
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41038
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/18-32677395-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677395
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677395
    reference: chr 18
allele count: 1
allele frequency: 8.466683600033867e-6
allele num: 118110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.122-15C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.215-15C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-64C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.251-15C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.122-15C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.122-15C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.122-15C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.251-15C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-15C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.122-15C>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
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: C
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: FS

18-32677397-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677397
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677397
    reference: chr 18
allele count: 2
allele frequency: 1.690874351126968e-5
allele num: 118282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.215-13T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-13T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-62T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.122-13T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.251-13T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.122-13T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.122-13T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.122-13T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.122-13T>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.251-13T>G
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14593
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3109
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

18-32677398-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677398
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677398
    reference: chr 18
allele count: 3
allele frequency: 2.535154137371552e-5
allele num: 118336
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.251-12G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.122-12G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.92-12G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.251-12G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-61G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.215-12G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.122-12G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.122-12G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.122-12G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.122-12G>T
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

18-32677414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677414
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677414
    reference: chr 18
allele count: 3
allele frequency: 2.509578223553228e-5
allele num: 119542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.219G>A
  hgvsp: ENST00000436190.2:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.255G>A
  hgvsp: ENST00000588910.1:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.126G>A
  hgvsp: ENST00000413393.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.126G>A
  hgvsp: ENST00000591734.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.126G>A
  hgvsp: ENST00000587359.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-45G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.255G>A
  hgvsp: ENST00000300249.5:c.255G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.96G>A
  hgvsp: ENST00000538170.2:c.96G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.126G>A
  hgvsp: ENST00000589699.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.126G>A
  hgvsp: ENST00000588349.2:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala85Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

18-32677426-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677426
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677426
    reference: chr 18
allele count: 8
allele frequency: 6.659341391136417e-5
allele num: 120132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.267A>G
  hgvsp: ENST00000588910.1:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.231A>G
  hgvsp: ENST00000436190.2:c.231A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.138A>G
  hgvsp: ENST00000413393.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.138A>G
  hgvsp: ENST00000587359.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.138A>G
  hgvsp: ENST00000591734.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.138A>G
  hgvsp: ENST00000589699.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.138A>G
  hgvsp: ENST00000588349.2:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.267A>G
  hgvsp: ENST00000300249.5:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-33A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.108A>G
  hgvsp: ENST00000538170.2:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln89Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-32677449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677449
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677449
    reference: chr 18
allele count: 1
allele frequency: 8.299581701082266e-6
allele num: 120488
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.290G>A
  hgvsp: ENSP00000468588.1:p.Gly97Asp
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.18-10G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.161G>A
  hgvsp: ENSP00000396074.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.161G>A
  hgvsp: ENSP00000468904.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.290G>A
  hgvsp: ENSP00000300249.4:p.Gly97Asp
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.161G>A
  hgvsp: ENSP00000466871.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.161G>A
  hgvsp: ENSP00000464921.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.131G>A
  hgvsp: ENSP00000446343.1:p.Gly44Asp
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.254G>A
  hgvsp: ENSP00000407723.1:p.Gly85Asp
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.161G>A
  hgvsp: ENSP00000468216.1:p.Gly54Asp
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly97Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

18-32677462-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677462
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677462
    reference: chr 18
allele count: 3
allele frequency: 2.488263689597399e-5
allele num: 120566
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.303G>A
  hgvsp: ENST00000300249.5:c.303G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.174G>A
  hgvsp: ENST00000587359.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.174G>A
  hgvsp: ENST00000588349.2:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.303G>A
  hgvsp: ENST00000588910.1:c.303G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.267G>A
  hgvsp: ENST00000436190.2:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.144G>A
  hgvsp: ENST00000538170.2:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.174G>A
  hgvsp: ENST00000589699.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.21G>A
  hgvsp: ENST00000589180.1:c.21G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.174G>A
  hgvsp: ENST00000413393.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.174G>A
  hgvsp: ENST00000591734.1:c.174G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu101Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-32677509-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677509
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677509
    reference: chr 18
allele count: 1
allele frequency: 8.368340892734607e-6
allele num: 119498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.350A>G
  hgvsp: ENSP00000468588.1:p.Asn117Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.221A>G
  hgvsp: ENSP00000464921.1:p.Asn74Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.221A>G
  hgvsp: ENSP00000468904.1:p.Asn74Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.68A>G
  hgvsp: ENSP00000465939.1:p.Asn23Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.221A>G
  hgvsp: ENSP00000396074.1:p.Asn74Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.350A>G
  hgvsp: ENSP00000300249.4:p.Asn117Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.221A>G
  hgvsp: ENSP00000466871.1:p.Asn74Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.221A>G
  hgvsp: ENSP00000468216.1:p.Asn74Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.191A>G
  hgvsp: ENSP00000446343.1:p.Asn64Ser
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.314A>G
  hgvsp: ENSP00000407723.1:p.Asn105Ser
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7336
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asn117Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

18-32677520-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677520
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677520
    reference: chr 18
allele count: 2
allele frequency: 1.683671751355356e-5
allele num: 118788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000466871
  ensembl transcript: ENST00000587359
  gene symbol: MAPRE2
  hgvsc: ENST00000587359.1:c.232C>T
  hgvsp: ENST00000587359.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.232C>T
  hgvsp: ENST00000591734.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.232C>T
  hgvsp: ENST00000589699.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.79C>T
  hgvsp: ENST00000589180.1:c.79C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.361C>T
  hgvsp: ENST00000588910.1:c.361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.232C>T
  hgvsp: ENST00000588349.2:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.202C>T
  hgvsp: ENST00000538170.2:c.202C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.361C>T
  hgvsp: ENST00000300249.5:c.361C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.232C>T
  hgvsp: ENST00000413393.1:c.232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.325C>T
  hgvsp: ENST00000436190.2:c.325C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu121Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-32677541-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677541
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677541
    reference: chr 18
allele count: 1
allele frequency: 8.647975508933359e-6
allele num: 115634
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.253A>G
  hgvsp: ENSP00000464921.1:p.Met85Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.253A>G
  hgvsp: ENSP00000396074.1:p.Met85Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.382A>G
  hgvsp: ENSP00000468588.1:p.Met128Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.253A>G
  hgvsp: ENSP00000468904.1:p.Met85Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.100A>G
  hgvsp: ENSP00000465939.1:p.Met34Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.223A>G
  hgvsp: ENSP00000446343.1:p.Met75Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.382A>G
  hgvsp: ENSP00000300249.4:p.Met128Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.253A>G
  hgvsp: ENSP00000468216.1:p.Met85Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.346A>G
  hgvsp: ENSP00000407723.1:p.Met116Val
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3023
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met128Val
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

18-32677546-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677546
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677546
    reference: chr 18
allele count: 2
allele frequency: 1.740825847782188e-5
allele num: 114888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.351C>T
  hgvsp: ENST00000436190.2:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.228C>T
  hgvsp: ENST00000538170.2:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.387C>T
  hgvsp: ENST00000588910.1:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.387C>T
  hgvsp: ENST00000300249.5:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.258C>T
  hgvsp: ENST00000413393.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.258C>T
  hgvsp: ENST00000588349.2:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.258C>T
  hgvsp: ENST00000589699.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.105C>T
  hgvsp: ENST00000589180.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.258C>T
  hgvsp: ENST00000591734.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25037
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39433
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn129Asn
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

18-32677547-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677547
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677547
    reference: chr 18
allele count: 2
allele frequency: 1.747885059078515e-5
allele num: 114424
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.259G>A
  hgvsp: ENSP00000464921.1:p.Val87Ile
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.229G>A
  hgvsp: ENSP00000446343.1:p.Val77Ile
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.352G>A
  hgvsp: ENSP00000407723.1:p.Val118Ile
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.388G>A
  hgvsp: ENSP00000300249.4:p.Val130Ile
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.259G>A
  hgvsp: ENSP00000468216.1:p.Val87Ile
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.106G>A
  hgvsp: ENSP00000465939.1:p.Val36Ile
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.259G>A
  hgvsp: ENSP00000396074.1:p.Val87Ile
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.388G>A
  hgvsp: ENSP00000468588.1:p.Val130Ile
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.259G>A
  hgvsp: ENSP00000468904.1:p.Val87Ile
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3283
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24724
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 793
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val130Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

18-32677558-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677558
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677558
    reference: chr 18
allele count: 1
allele frequency: 8.941984405179198e-6
allele num: 111832
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+3A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+3A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+3A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+3A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+3A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+3A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+3A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+3A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+3A>G
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14573
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7430
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1333
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4685
  bin: 6.75e1
  variant carriers: 0
hgvs: c.396+3A>G
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum

18-32677564-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677564
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677564
    reference: chr 18
allele count: 1
allele frequency: 9.127085539045672e-6
allele num: 109564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+9C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+9C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+9C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+9C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+9C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+9C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+9C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+9C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+9C>T
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10449
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12584
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1925
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

18-32677566-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677566
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677566
    reference: chr 18
allele count: 1
allele frequency: 9.19337341644143e-6
allele num: 108774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+11T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+11T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+11T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+11T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+11T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+11T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+11T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+11T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+11T>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20031
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2230
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

18-32677567-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677567
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677567
    reference: chr 18
allele count: 1
allele frequency: 9.201494322678003e-6
allele num: 108678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+12G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+12G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+12G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+12G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+12G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+12G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+12G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+12G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+12G>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11814
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29879
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4057
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13729
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

18-32677568-T-TACCTC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677568
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677573
    reference: chr 18
allele count: 2
allele frequency: 1.845665454679685e-5
allele num: 108362
alternate allele: TACCTC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+14_267+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+14_267+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+14_396+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+14_237+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+14_396+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+14_114+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+14_267+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+14_267+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+14_360+18dupACCTC
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10950
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19547
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14305
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/18-32677573-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677573
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677573
    reference: chr 18
allele count: 3
allele frequency: 2.819707878263812e-5
allele num: 106394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+18C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+18C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+18C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+18C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+18C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+18C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+18C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+18C>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+18C>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17236
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25097
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3125
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

18-32677576-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677576
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677576
    reference: chr 18
allele count: 1
allele frequency: 9.503535315137231e-6
allele num: 105224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+21T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+21T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+21T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+21T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+21T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+21T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+21T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+21T>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+21T>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7085
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15090
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

18-32677581-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677581
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677581
    reference: chr 18
allele count: 1
allele frequency: 9.632983334938831e-6
allele num: 103810
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+26T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+26T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+26T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+26T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+26T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+26T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+26T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+26T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+26T>C
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4742
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

18-32677584-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677584
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677584
    reference: chr 18
allele count: 4
allele frequency: 3.89120199229542e-5
allele num: 102796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+29G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+29G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+29G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+29G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+29G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+29G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+29G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+29G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+29G>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6588
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10462
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7733
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1487
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6417
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2988
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14751
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP

18-32677585-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677585
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677585
    reference: chr 18
allele count: 1
allele frequency: 9.847171892232552e-6
allele num: 101552
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+30T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+30T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+30T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+30T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+30T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+30T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+30T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+30T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+30T>C
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8018
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22746
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4482
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2983
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5339
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum

18-32677587-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677587
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677588
    reference: chr 18
allele count: 1
allele frequency: 9.877128521196317e-6
allele num: 101244
alternate allele: GT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+38dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+38dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+38dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+38dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+38dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+38dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+38dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+38dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+38dupT
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8760
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19652
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

18-32677602-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32677602
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32677602
    reference: chr 18
allele count: 1
allele frequency: 1.086838387131833e-5
allele num: 92010
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.267+47T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.267+47T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.396+47T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.267+47T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.396+47T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.237+47T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.360+47T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.114+47T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.267+47T>C
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19956
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12068
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5607
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2844
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14742
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8570
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5488
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

18-32681860-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681860
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681860
    reference: chr 18
allele count: 2
allele frequency: 1.853430700226118e-5
allele num: 107908
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.268-50A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.268-50A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.397-50A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.238-50A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.268-50A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.268-50A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.397-50A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.361-50A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.115-50A>G
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16275
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5843
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3650
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

18-32681862-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681862
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681862
    reference: chr 18
allele count: 4
allele frequency: 3.703635117868187e-5
allele num: 108002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.238-48A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.115-48A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.268-48A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.268-48A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.268-48A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.397-48A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.361-48A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.397-48A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.268-48A>G
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5284
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15321
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2699
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25753
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

18-32681874-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681874
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681874
    reference: chr 18
allele count: 38
allele frequency: 3.501723216424925e-4
allele num: 108518
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.268-36G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.268-36G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.397-36G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.397-36G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.268-36G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.268-36G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.361-36G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.115-36G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.238-36G>T
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22165
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17870
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

18-32681876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681876
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681876
    reference: chr 18
allele count: 2
allele frequency: 1.840163406510498e-5
allele num: 108686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.268-34G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.397-34G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.361-34G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.238-34G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.268-34G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.268-34G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.268-34G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.397-34G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.115-34G>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18116
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 809
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1218
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

18-32681896-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681896
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681897
    reference: chr 18
allele count: 24
allele frequency: 2.168922949012236e-4
allele num: 110654
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.268-8dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.268-8dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.268-8dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.238-8dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.361-8dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.397-8dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.268-8dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.397-8dupT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.115-8dupT
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24495
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 19129
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3180
  bin: 9.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4251
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

18-32681896-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681896
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681896
    reference: chr 18
allele count: 2
allele frequency: 1.80743579084353e-5
allele num: 110654
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.268-14A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.361-14A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.115-14A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.397-14A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.397-14A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.238-14A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.268-14A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.268-14A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.268-14A>G
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 7.5e0
  variant carriers: 0
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: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

18-32681903-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681903
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681903
    reference: chr 18
allele count: 1
allele frequency: 8.993938085730218e-6
allele num: 111186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.397-7A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.268-7A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.361-7A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.238-7A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.115-7A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.268-7A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.397-7A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.268-7A>G
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.268-7A>G
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39553
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
hgvs: c.397-7A>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

18-32681904-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681904
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681904
    reference: chr 18
allele count: 1
allele frequency: 8.98311174991017e-6
allele num: 111320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.115-6T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.268-6T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.268-6T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.397-6T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.361-6T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.397-6T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.268-6T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.268-6T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.238-6T>C
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39678
  bin: 6.25e1
  variant carriers: 0
hgvs: c.397-6T>C
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

18-32681912-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681912
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681912
    reference: chr 18
allele count: 1
allele frequency: 8.881941237076776e-6
allele num: 112588
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.399A>G
  hgvsp: ENST00000588910.1:c.399A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.270A>G
  hgvsp: ENST00000591734.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.240A>G
  hgvsp: ENST00000538170.2:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.270A>G
  hgvsp: ENST00000413393.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.399A>G
  hgvsp: ENST00000300249.5:c.399A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.363A>G
  hgvsp: ENST00000436190.2:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.270A>G
  hgvsp: ENST00000588349.2:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.270A>G
  hgvsp: ENST00000589699.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.117A>G
  hgvsp: ENST00000589180.1:c.117A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
hgvs: c.399A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

18-32681921-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681921
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681921
    reference: chr 18
allele count: 4
allele frequency: 3.506680225830207e-5
allele num: 114068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.408G>A
  hgvsp: ENST00000588910.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.279G>A
  hgvsp: ENST00000588349.2:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.249G>A
  hgvsp: ENST00000538170.2:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.408G>A
  hgvsp: ENST00000300249.5:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.126G>A
  hgvsp: ENST00000589180.1:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.279G>A
  hgvsp: ENST00000591734.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.279G>A
  hgvsp: ENST00000589699.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.372G>A
  hgvsp: ENST00000436190.2:c.372G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.279G>A
  hgvsp: ENST00000413393.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val136Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

18-32681949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681949
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681949
    reference: chr 18
allele count: 1
allele frequency: 8.430992327796981e-6
allele num: 118610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.400G>A
  hgvsp: ENSP00000407723.1:p.Asp134Asn
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.154G>A
  hgvsp: ENSP00000465939.1:p.Asp52Asn
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.307G>A
  hgvsp: ENSP00000468904.1:p.Asp103Asn
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.307G>A
  hgvsp: ENSP00000396074.1:p.Asp103Asn
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.436G>A
  hgvsp: ENSP00000300249.4:p.Asp146Asn
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.436G>A
  hgvsp: ENSP00000468588.1:p.Asp146Asn
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.277G>A
  hgvsp: ENSP00000446343.1:p.Asp93Asn
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.307G>A
  hgvsp: ENSP00000464921.1:p.Asp103Asn
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.307G>A
  hgvsp: ENSP00000468216.1:p.Asp103Asn
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp146Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum

18-32681978-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32681978
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32681978
    reference: chr 18
allele count: 1
allele frequency: 8.291048983517394e-6
allele num: 120612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.336G>A
  hgvsp: ENST00000589699.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.465G>A
  hgvsp: ENST00000300249.5:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.336G>A
  hgvsp: ENST00000591734.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.183G>A
  hgvsp: ENST00000589180.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.465G>A
  hgvsp: ENST00000588910.1:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.429G>A
  hgvsp: ENST00000436190.2:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.306G>A
  hgvsp: ENST00000538170.2:c.306G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.336G>A
  hgvsp: ENST00000413393.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.336G>A
  hgvsp: ENST00000588349.2:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20532
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys155Lys
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

18-32682002-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682002
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682002
    reference: chr 18
allele count: 1
allele frequency: 8.271845945141119e-6
allele num: 120892
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.489T>C
  hgvsp: ENST00000588910.1:c.489T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.360T>C
  hgvsp: ENST00000589699.1:c.360T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.489T>C
  hgvsp: ENST00000300249.5:c.489T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.330T>C
  hgvsp: ENST00000538170.2:c.330T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.207T>C
  hgvsp: ENST00000589180.1:c.207T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.453T>C
  hgvsp: ENST00000436190.2:c.453T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.360T>C
  hgvsp: ENST00000591734.1:c.360T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.360T>C
  hgvsp: ENST00000413393.1:c.360T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.360T>C
  hgvsp: ENST00000588349.2:c.360T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6896
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp163Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

18-32682011-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682011
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682011
    reference: chr 18
allele count: 1
allele frequency: 8.271845945141119e-6
allele num: 120892
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.498G>A
  hgvsp: ENST00000300249.5:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.462G>A
  hgvsp: ENST00000436190.2:c.462G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.216G>A
  hgvsp: ENST00000589180.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.498G>A
  hgvsp: ENST00000588910.1:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.339G>A
  hgvsp: ENST00000538170.2:c.339G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.369G>A
  hgvsp: ENST00000589699.1:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.369G>A
  hgvsp: ENST00000591734.1:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468904
  ensembl transcript: ENST00000588349
  gene symbol: MAPRE2
  hgvsc: ENST00000588349.2:c.369G>A
  hgvsp: ENST00000588349.2:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.369G>A
  hgvsp: ENST00000413393.1:c.369G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28854
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu166Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

18-32682025-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682025
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682025
    reference: chr 18
allele count: 1
allele frequency: 8.277186418792524e-6
allele num: 120814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.230A>G
  hgvsp: ENSP00000465939.1:p.Glu77Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.353A>G
  hgvsp: ENSP00000446343.1:p.Glu118Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.512A>G
  hgvsp: ENSP00000468588.1:p.Glu171Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.383A>G
  hgvsp: ENSP00000396074.1:p.Glu128Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.476A>G
  hgvsp: ENSP00000407723.1:p.Glu159Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.512A>G
  hgvsp: ENSP00000300249.4:p.Glu171Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.383A>G
  hgvsp: ENSP00000464921.1:p.Glu128Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.383A>G
  hgvsp: ENSP00000468216.1:p.Glu128Gly
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20776
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu171Gly
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

18-32682033-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682033
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682033
    reference: chr 18
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.391C>G
  hgvsp: ENSP00000468216.1:p.Gln131Glu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.391C>G
  hgvsp: ENSP00000396074.1:p.Gln131Glu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.520C>G
  hgvsp: ENSP00000300249.4:p.Gln174Glu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.391C>G
  hgvsp: ENSP00000464921.1:p.Gln131Glu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.520C>G
  hgvsp: ENSP00000468588.1:p.Gln174Glu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.484C>G
  hgvsp: ENSP00000407723.1:p.Gln162Glu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.238C>G
  hgvsp: ENSP00000465939.1:p.Gln80Glu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.361C>G
  hgvsp: ENSP00000446343.1:p.Gln121Glu
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20798
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln174Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP

18-32682048-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682048
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682048
    reference: chr 18
allele count: 2
allele frequency: 1.659117681217129e-5
allele num: 120546
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.535A>G
  hgvsp: ENSP00000300249.4:p.Ile179Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.499A>G
  hgvsp: ENSP00000407723.1:p.Ile167Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.376A>G
  hgvsp: ENSP00000446343.1:p.Ile126Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.406A>G
  hgvsp: ENSP00000464921.1:p.Ile136Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.406A>G
  hgvsp: ENSP00000396074.1:p.Ile136Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.406A>G
  hgvsp: ENSP00000468216.1:p.Ile136Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.535A>G
  hgvsp: ENSP00000468588.1:p.Ile179Val
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.253A>G
  hgvsp: ENSP00000465939.1:p.Ile85Val
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3160
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile179Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

18-32682062-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682062
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682062
    reference: chr 18
allele count: 1
allele frequency: 8.335278231587371e-6
allele num: 119972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.390C>T
  hgvsp: ENST00000538170.2:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.420C>T
  hgvsp: ENST00000591734.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.420C>T
  hgvsp: ENST00000413393.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.420C>T
  hgvsp: ENST00000589699.1:c.420C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.549C>T
  hgvsp: ENST00000588910.1:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.513C>T
  hgvsp: ENST00000436190.2:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.549C>T
  hgvsp: ENST00000300249.5:c.549C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.267C>T
  hgvsp: ENST00000589180.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3159
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp183Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-32682068-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682068
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682068
    reference: chr 18
allele count: 1
allele frequency: 8.355056480181806e-6
allele num: 119688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.519T>A
  hgvsp: ENST00000436190.2:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.273T>A
  hgvsp: ENST00000589180.1:c.273T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.555T>A
  hgvsp: ENST00000588910.1:c.555T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.426T>A
  hgvsp: ENST00000591734.1:c.426T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.555T>A
  hgvsp: ENST00000300249.5:c.555T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.426T>A
  hgvsp: ENST00000589699.1:c.426T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.426T>A
  hgvsp: ENST00000413393.1:c.426T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.396T>A
  hgvsp: ENST00000538170.2:c.396T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly185Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

18-32682068-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682068
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682068
    reference: chr 18
allele count: 52
allele frequency: 4.344629369694539e-4
allele num: 119688
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.426T>C
  hgvsp: ENST00000589699.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.555T>C
  hgvsp: ENST00000300249.5:c.555T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.273T>C
  hgvsp: ENST00000589180.1:c.273T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.396T>C
  hgvsp: ENST00000538170.2:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.426T>C
  hgvsp: ENST00000413393.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.555T>C
  hgvsp: ENST00000588910.1:c.555T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.519T>C
  hgvsp: ENST00000436190.2:c.519T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.426T>C
  hgvsp: ENST00000591734.1:c.426T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27321
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20668
  bin: 2.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43387
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly185Gly
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-32682074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682074
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682074
    reference: chr 18
allele count: 1
allele frequency: 8.378437253883405e-6
allele num: 119354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.432G>A
  hgvsp: ENST00000591734.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.402G>A
  hgvsp: ENST00000538170.2:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.432G>A
  hgvsp: ENST00000589699.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.432G>A
  hgvsp: ENST00000413393.1:c.432G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.525G>A
  hgvsp: ENST00000436190.2:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.561G>A
  hgvsp: ENST00000300249.5:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.561G>A
  hgvsp: ENST00000588910.1:c.561G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.279G>A
  hgvsp: ENST00000589180.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln187Gln
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

18-32682112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682112
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682112
    reference: chr 18
allele count: 1
allele frequency: 8.682515150988938e-6
allele num: 115174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.470C>T
  hgvsp: ENSP00000464921.1:p.Ser157Phe
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.563C>T
  hgvsp: ENSP00000407723.1:p.Ser188Phe
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.317C>T
  hgvsp: ENSP00000465939.1:p.Ser106Phe
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.599C>T
  hgvsp: ENSP00000468588.1:p.Ser200Phe
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.440C>T
  hgvsp: ENSP00000446343.1:p.Ser147Phe
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.470C>T
  hgvsp: ENSP00000468216.1:p.Ser157Phe
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.599C>T
  hgvsp: ENSP00000300249.4:p.Ser200Phe
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.470C>T
  hgvsp: ENSP00000396074.1:p.Ser157Phe
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19941
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3150
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser200Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-32682115-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682115
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682115
    reference: chr 18
allele count: 1
allele frequency: 8.719003940989781e-6
allele num: 114692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.320C>T
  hgvsp: ENSP00000465939.1:p.Pro107Leu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.473C>T
  hgvsp: ENSP00000468216.1:p.Pro158Leu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.602C>T
  hgvsp: ENSP00000300249.4:p.Pro201Leu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.473C>T
  hgvsp: ENSP00000396074.1:p.Pro158Leu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.566C>T
  hgvsp: ENSP00000407723.1:p.Pro189Leu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.602C>T
  hgvsp: ENSP00000468588.1:p.Pro201Leu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.443C>T
  hgvsp: ENSP00000446343.1:p.Pro148Leu
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.473C>T
  hgvsp: ENSP00000464921.1:p.Pro158Leu
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19913
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro201Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS

18-32682121-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682121
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682121
    reference: chr 18
allele count: 1
allele frequency: 8.813834194151139e-6
allele num: 113458
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.608C>G
  hgvsp: ENSP00000300249.4:p.Ala203Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.449C>G
  hgvsp: ENSP00000446343.1:p.Ala150Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.479C>G
  hgvsp: ENSP00000468216.1:p.Ala160Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.326C>G
  hgvsp: ENSP00000465939.1:p.Ala109Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.572C>G
  hgvsp: ENSP00000407723.1:p.Ala191Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.479C>G
  hgvsp: ENSP00000464921.1:p.Ala160Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.608C>G
  hgvsp: ENSP00000468588.1:p.Ala203Gly
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.479C>G
  hgvsp: ENSP00000396074.1:p.Ala160Gly
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39221
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala203Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

18-32682139-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682139
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682139
    reference: chr 18
allele count: 4
allele frequency: 3.637091054574551e-5
allele num: 109978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.481+16G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.574+16G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.481+16G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.328+16G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.481+16G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.610+16G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.610+16G>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.451+16G>C
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34051
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6045
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

18-32682143-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682143
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682143
    reference: chr 18
allele count: 5
allele frequency: 4.591874219381383e-5
allele num: 108888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.481+20G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.610+20G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.328+20G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.481+20G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.451+20G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.481+20G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.574+20G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.610+20G>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18169
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3144
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4935
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

18-32682145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682145
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682145
    reference: chr 18
allele count: 2
allele frequency: 1.844099802681321e-5
allele num: 108454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.574+22G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.328+22G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.481+22G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.481+22G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.610+22G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.610+22G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.481+22G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.451+22G>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17133
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2332
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2513
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7009
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

18-32682147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682147
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682147
    reference: chr 18
allele count: 1
allele frequency: 9.2397531137968e-6
allele num: 108228
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.610+24G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.481+24G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.481+24G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.610+24G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.451+24G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.481+24G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.574+24G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.328+24G>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29752
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7354
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

18-32682149-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682149
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682149
    reference: chr 18
allele count: 371
allele frequency: 3.438687552136435e-3
allele num: 107890
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.451+26G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.481+26G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.574+26G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.481+26G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.610+26G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.610+26G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.481+26G>A
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.328+26G>A
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 3.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16345
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.25e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 15748
  bin: 2.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 8871
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4039
  bin: 1.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1969
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 4.75e1
  variant carriers: 1
num of homozygotes: 6
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

18-32682172-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32682172
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32682172
    reference: chr 18
allele count: 14
allele frequency: 1.357536265611667e-4
allele num: 103128
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.481+49C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.481+49C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.610+49C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.610+49C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.328+49C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.481+49C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.574+49C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.451+49C>T
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6808
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10403
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14384
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13758
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1681
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6442
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6716
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6573
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

18-32706878-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32706878
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32706878
    reference: chr 18
allele count: 1
allele frequency: 8.466396870819716e-6
allele num: 118114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.452-34G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.575-34G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.482-34G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.611-34G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.482-34G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.482-34G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.611-34G>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.329-34G>T
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11536
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1088
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

18-32706880-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32706880
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32706880
    reference: chr 18
allele count: 1
allele frequency: 8.45809016324114e-6
allele num: 118230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.575-32C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.611-32C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.482-32C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.329-32C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.482-32C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.482-32C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.452-32C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.611-32C>T
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18017
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14589
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

18-32706890-CATTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32706890
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32706886
    reference: chr 18
allele count: 12
allele frequency: 1.008369466572552e-4
allele num: 119004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.611-18_611-15delTATT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.575-18_575-15delTATT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.452-18_452-15delTATT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.482-18_482-15delTATT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.482-18_482-15delTATT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.611-18_611-15delTATT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.329-18_329-15delTATT
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.482-18_482-15delTATT
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18474
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11614
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: CATTT
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

18-32706898-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32706898
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32706898
    reference: chr 18
allele count: 1
allele frequency: 8.349475652928997e-6
allele num: 119768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.482-14C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.452-14C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.575-14C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.611-14C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.329-14C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.611-14C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.482-14C>T
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.482-14C>T
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6591
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3655
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

18-32706899-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 32706899
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 32706899
    reference: chr 18
allele count: 2
allele frequency: 1.6679454248257e-5
allele num: 119908
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000407723
  ensembl transcript: ENST00000436190
  gene symbol: MAPRE2
  hgvsc: ENST00000436190.2:c.575-13T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468216
  ensembl transcript: ENST00000591734
  gene symbol: MAPRE2
  hgvsc: ENST00000591734.1:c.482-13T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000464921
  ensembl transcript: ENST00000589699
  gene symbol: MAPRE2
  hgvsc: ENST00000589699.1:c.482-13T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000468588
  ensembl transcript: ENST00000588910
  gene symbol: MAPRE2
  hgvsc: ENST00000588910.1:c.611-13T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000465939
  ensembl transcript: ENST00000589180
  gene symbol: MAPRE2
  hgvsc: ENST00000589180.1:c.329-13T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000300249
  ensembl transcript: ENST00000300249
  gene symbol: MAPRE2
  hgvsc: ENST00000300249.5:c.611-13T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000396074
  ensembl transcript: ENST00000413393
  gene symbol: MAPRE2
  hgvsc: ENST00000413393.1:c.482-13T>C
  variant of: http://identifiers.org/hgnc/6891
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166974
  ensembl protein: ENSP00000446343
  ensembl transcript: ENST00000538170
  gene symbol: MAPRE2
  hgvsc: ENST00000538170.2:c.452-13T>C
  variant of: http://identifiers.org/hgnc/6891
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 4352
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6399
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15463
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3146
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4939
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2223
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.906413485758574e-4
allele num: 10322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.925e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

MQ
type: SiteQuality
SIO_000300: 5.879e1

MQRankSum
type: SiteQuality
SIO_000300: 8.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

QD
type: SiteQuality
SIO_000300: 2.9e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

DP
type: SiteQuality
SIO_000300: 2.109315e6

FS
type: SiteQuality
SIO_000300: 1.971e0

GenotypeQuality
all individuals: 4962
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2873
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15244
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6377
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3150
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2237
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15528
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 747
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.563154052080798e-5
allele num: 65744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.49e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

FS
type: SiteQuality
SIO_000300: 7.703e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.094927e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

QD
type: SiteQuality
SIO_000300: 1.394e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

GenotypeQuality
all individuals: 3443
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15525
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3132
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14221
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.609603340292275e-4
allele num: 11496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65628
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14026
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.919e1

QD
type: SiteQuality
SIO_000300: 1.339e1

FS
type: SiteQuality
SIO_000300: 3.957e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.8e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.601e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.91e-1

DP
type: SiteQuality
SIO_000300: 2.080108e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

GenotypeQuality
all individuals: 3435
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2636
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4839
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 755
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15531
bin: 9.75e1
variant carriers: 35

GenotypeQuality
all individuals: 1297
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1492
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5865
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4333
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3019
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10487
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 34
allele frequency: 3.331373701744072e-3
allele num: 10206
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13240
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.95e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

DP
type: SiteQuality
SIO_000300: 2.044244e6

FS
type: SiteQuality
SIO_000300: 9.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

QD
type: SiteQuality
SIO_000300: 1.454e1

GenotypeQuality
all individuals: 15510
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1465
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3437
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4331
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4807
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5840
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532520076012996e-5
allele num: 65252
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13124
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.28e0

DP
type: SiteQuality
SIO_000300: 2.041441e6

QD
type: SiteQuality
SIO_000300: 1.964e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.831e0

MQRankSum
type: SiteQuality
SIO_000300: 4.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

GenotypeQuality
all individuals: 5520
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15511
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1605
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2217
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7562
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2990
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2231
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4796
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4323
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2133
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.535107918086642e-5
allele num: 65142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.328e1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e0

DP
type: SiteQuality
SIO_000300: 2.029922e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

GenotypeQuality
all individuals: 2124
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3436
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 386
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2230
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5535
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3000
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15523
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 4804
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2215
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4326
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 2.609363008442057e-4
allele num: 65150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12868
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10166
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.264e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.182e0

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-2

QD
type: SiteQuality
SIO_000300: 1.267e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e-1

DP
type: SiteQuality
SIO_000300: 2.029438e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532942943863629e-5
allele num: 65234
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.703699e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.292e1

MQRankSum
type: SiteQuality
SIO_000300: 1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.31e0

GenotypeQuality
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variant carriers: 2

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.064194882794546e-5
allele num: 65270
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10100
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Latino
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allele frequency: 0.0e0
allele num: 11422
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 14498
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.762e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.241e0

DP
type: SiteQuality
SIO_000300: 1.710741e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
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SIO_000300: 1.2756e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.286e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532097441397273e-5
allele num: 65270
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.286e0

MQRankSum
type: SiteQuality
SIO_000300: -7.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.762e0

DP
type: SiteQuality
SIO_000300: 1.710741e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.053e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.241e0

FS
type: SiteQuality
SIO_000300: 1.2756e1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10110
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.529613313754283e-5
allele num: 65376
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.717725e6

FS
type: SiteQuality
SIO_000300: 8.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 8.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.537e0

QD
type: SiteQuality
SIO_000300: 1.107e1

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
all individuals: 106
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65462
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.656903208627346e-5
allele num: 15022
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.727081e6

VQSLOD
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.86e-1

QD
type: SiteQuality
SIO_000300: 1.174e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

FS
type: SiteQuality
SIO_000300: 7.085e0

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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GenotypeQuality
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GenotypeQuality
all individuals: 1000
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15138
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.052689419378472e-5
allele num: 65516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.5912e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

DP
type: SiteQuality
SIO_000300: 1.728988e6

QD
type: SiteQuality
SIO_000300: 1.742e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
SIO_000300: -1.875e0

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.052316708381662e-5
allele num: 65524
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.587615283267457e-5
allele num: 15180
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.135e0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.399e1

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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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
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: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.036375781866764e-5
allele num: 65868
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.83477576711251e-5
allele num: 10168
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15966
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.74956e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.12e-1

VQSLOD
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MQ
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
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SIO_000300: 2.461e0

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1731
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1007
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7144
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1877
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44023
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.452483139178418e-4
allele num: 16310
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.719916288803627e-5
allele num: 11468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.542013626040878e-5
allele num: 66050
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.83e0

QD
type: SiteQuality
SIO_000300: 1.319e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.136e0

DP
type: SiteQuality
SIO_000300: 1.757201e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e-1

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1736
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3095
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7153
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44313
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509844184080203e-5
allele num: 66232
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.05e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.899e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 3.35e0

VQSLOD
type: SiteQuality
SIO_000300: -4.968e0

FS
type: SiteQuality
SIO_000300: 3.408e0

DP
type: SiteQuality
SIO_000300: 1.760602e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.382e0

GenotypeQuality
all individuals: 44349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1719
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3091
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 996
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1864
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7124
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 328
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.078288353999514e-5
allele num: 16452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508477644361311e-5
allele num: 66292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.176e1

FS
type: SiteQuality
SIO_000300: 1.065e0

MQRankSum
type: SiteQuality
SIO_000300: 4.69e-1

DP
type: SiteQuality
SIO_000300: 1.759567e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.973e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

GenotypeQuality
all individuals: 237
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43144
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 169
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1482
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3046
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 296
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.752291788570315e-5
allele num: 10254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.2654e1

VQSLOD
type: SiteQuality
SIO_000300: -2.667e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.713089e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.49e-1

QD
type: SiteQuality
SIO_000300: 9.9e-1

GenotypeQuality
all individuals: 857
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6193
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42398
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 288
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3041
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 377
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16018
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.058384561274735e-5
allele num: 65394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.695719e6

FS
type: SiteQuality
SIO_000300: 1.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.071e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.126e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

GenotypeQuality
all individuals: 129
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5527
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 5250
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 635
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 568
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39602
bin: 6.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.729475100942126e-5
allele num: 14860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63958
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11052
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.451e0

DP
type: SiteQuality
SIO_000300: 1.630166e6

FS
type: SiteQuality
SIO_000300: 2.674e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

QD
type: SiteQuality
SIO_000300: 1.852e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.9e-1

GenotypeQuality
all individuals: 1217
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
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GenotypeQuality
all individuals: 5963
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3019
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 5329
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 322
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1105
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.57257430413587e-5
allele num: 63590
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.09090909090909e-5
allele num: 11000
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 4.769e0

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.29e0

DP
type: SiteQuality
SIO_000300: 1.61671e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 428
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6569
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3016
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1171
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38558
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.378929950358522e-4
allele num: 14504
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9930
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63368
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2449e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.604613e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.91e-1

QD
type: SiteQuality
SIO_000300: 5.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.9e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.609e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62054
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.233796296296296e-5
allele num: 13824
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

DP
type: SiteQuality
SIO_000300: 1.537586e6

VQSLOD
type: SiteQuality
SIO_000300: 5.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.315e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

QD
type: SiteQuality
SIO_000300: 1.531e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.03e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.643871646501841e-5
allele num: 60832
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.192e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.98e-1

DP
type: SiteQuality
SIO_000300: 1.476411e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.128e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.103e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60402
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.589566551591868e-5
allele num: 10428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8062
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.314e0

DP
type: SiteQuality
SIO_000300: 1.449854e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.552e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQRankSum
type: SiteQuality
SIO_000300: -1.505e0

MQ
type: SiteQuality
SIO_000300: 5.631e1

QD
type: SiteQuality
SIO_000300: 8.779999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.11e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.656561640658649e-5
allele num: 60366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13140
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 5.92e0

DP
type: SiteQuality
SIO_000300: 1.448988e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.995e-1

MQ
type: SiteQuality
SIO_000300: 5.604e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.9e-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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.322700691121744e-5
allele num: 60192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8026
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13068
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.434749e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.98e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.192e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.308e0

QD
type: SiteQuality
SIO_000300: 6.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
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: 800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.069108850664053e-5
allele num: 59182
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7890
num of homozygotes: 0

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

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.6e-3

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 1
allele frequency: 1.280081925243216e-4
allele num: 7812
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58598
num of homozygotes: 0

European (Finnish)
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allele count: 0
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BaseQRankSum
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MQRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -2.4e-3

VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.077354018530489e-4
allele num: 9282
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11880
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 8.149999999999999e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 557
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 57414
num of homozygotes: 0

European (Finnish)
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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: 784
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 11588
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 4.031445273130417e-4
allele num: 9922
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -3.3e-3

MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

FS
type: SiteQuality
SIO_000300: 2.047e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.206542e6

GenotypeQuality
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bin: 7.5e0
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: 1.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56736
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9160
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7622
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.018537380321858e-4
allele num: 9818
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6160
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
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InbreedingCoeff
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SIO_000300: -3.7e-3

QD
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ClippingRankSum
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SIO_000300: 6.23e-1

VQSLOD
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MQRankSum
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MQ
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DP
type: SiteQuality
SIO_000300: 1.170563e6

FS
type: SiteQuality
SIO_000300: 1.2013e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

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: 1.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9122
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.767471455335996e-5
allele num: 56578
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7606
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6144
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.138e1

VQSLOD
type: SiteQuality
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MQRankSum
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.903e0

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.39e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

DP
type: SiteQuality
SIO_000300: 1.168393e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
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allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51632
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.118818527634818e-4
allele num: 8938
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9294
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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

MQRankSum
type: SiteQuality
SIO_000300: 9.59e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.005e-1

DP
type: SiteQuality
SIO_000300: 1.055766e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.452e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.244e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.198157861072023e-5
allele num: 62536
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9566
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VQSLOD
type: SiteQuality
SIO_000300: 6.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

DP
type: SiteQuality
SIO_000300: 1.407045e6

QD
type: SiteQuality
SIO_000300: 1.141e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.390184676337147e-5
allele num: 62596
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

FS
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

BaseQRankSum
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VQSLOD
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DP
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 37
allele frequency: 5.891344500350296e-4
allele num: 62804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 8.874689385871494e-5
allele num: 11268
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South Asian
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Other
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InbreedingCoeff
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FS
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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MQRankSum
type: SiteQuality
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DP
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QD
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

African
type: Population
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East Asian
type: Population
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allele frequency: 0.0e0
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Latino
type: Population
allele count: 2
allele frequency: 1.773049645390071e-4
allele num: 11280
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South Asian
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allele frequency: 0.0e0
allele num: 9280
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62882
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Other
type: Population
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QD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.881e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 3.019323671497584e-4
allele num: 9936
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Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.070663811563169e-3
allele num: 6538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
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European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 2.040624117037642e-4
allele num: 63706
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Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
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FS
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VQSLOD
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

QD
type: SiteQuality
SIO_000300: 1.105e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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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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variant carriers: 2

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1563
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9884
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.18427285646613e-4
allele num: 8444
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.809020436927414e-5
allele num: 11352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63706
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

QD
type: SiteQuality
SIO_000300: 1.105e1

DP
type: SiteQuality
SIO_000300: 1.533252e6

GenotypeQuality
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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
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564651395669045e-5
allele num: 63912
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.57e-1

FS
type: SiteQuality
SIO_000300: 6.186e0

DP
type: SiteQuality
SIO_000300: 1.539923e6

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

QD
type: SiteQuality
SIO_000300: 1.487e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

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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bin: 9.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9954
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.775171065493646e-5
allele num: 10230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63948
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.571e1

VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.67e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.893e0

DP
type: SiteQuality
SIO_000300: 1.540781e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

FS
type: SiteQuality
SIO_000300: 2.887e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

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

GenotypeQuality
all individuals: 206
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10078
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.175364362952515e-4
allele num: 8508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10912
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.435e0

QD
type: SiteQuality
SIO_000300: 1.179e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.581e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.5e0

DP
type: SiteQuality
SIO_000300: 1.552533e6

MQ
type: SiteQuality
SIO_000300: 5.954e1

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: 4

GenotypeQuality
all individuals: 391
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GenotypeQuality
all individuals: 87
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.934684241589612e-4
allele num: 10166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11786
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64716
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.277e0

MQRankSum
type: SiteQuality
SIO_000300: 7.13e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

VQSLOD
type: SiteQuality
SIO_000300: 2.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 3.194e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.39e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

DP
type: SiteQuality
SIO_000300: 1.565212e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518003521768171e-5
allele num: 65876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14810
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.61e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

DP
type: SiteQuality
SIO_000300: 1.607697e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 3.043e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.104e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16124
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504981488727689e-5
allele num: 66446
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.627687e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.587e0

MQ
type: SiteQuality
SIO_000300: 5.986e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.21e-1

GenotypeQuality
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bin: 1.25e1
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
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 4.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.29e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.82e-1

DP
type: SiteQuality
SIO_000300: 1.631725e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3161
bin: 9.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 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: 1
allele frequency: 1.503126503126503e-5
allele num: 66528
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.29e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 3.165e0

DP
type: SiteQuality
SIO_000300: 1.63202e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.264e0

MQRankSum
type: SiteQuality
SIO_000300: -3.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

GenotypeQuality
all individuals: 1589
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 6878
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variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

European (Finnish)
type: Population
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: 16210
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.292999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

DP
type: SiteQuality
SIO_000300: 1.630805e6

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.919e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.552e1

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

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
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: 16150
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503849855630414e-5
allele num: 66496
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -4.115e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.442e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.184e1

FS
type: SiteQuality
SIO_000300: 1.9335e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e0

DP
type: SiteQuality
SIO_000300: 1.630325e6

GenotypeQuality
all individuals: 104
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1582
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variant carriers: 0

GenotypeQuality
all individuals: 6859
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505208019748329e-5
allele num: 66436
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.239081607187422e-5
allele num: 16028
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.05e-1

QD
type: SiteQuality
SIO_000300: 1.484e1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 2.879e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.627174e6

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 7.75e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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: 1.508295625942685e-5
allele num: 66300
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15606
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.392e0

FS
type: SiteQuality
SIO_000300: 6.651e0

QD
type: SiteQuality
SIO_000300: 1.032e1

MQRankSum
type: SiteQuality
SIO_000300: -2.9e-1

DP
type: SiteQuality
SIO_000300: 1.618822e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.747e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 947
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variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Finnish)
type: Population
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: 15438
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.213e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.7e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

DP
type: SiteQuality
SIO_000300: 1.616178e6

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.89e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 52

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1568
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.469210754553339e-4
allele num: 11530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

African
type: Population
allele count: 13
allele frequency: 1.251684960523782e-3
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.510710940568632e-4
allele num: 66194
num of homozygotes: 0

South Asian
type: Population
allele count: 25
allele frequency: 1.619380748801658e-3
allele num: 15438
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.616178e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.89e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

QD
type: SiteQuality
SIO_000300: 1.213e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.7e-1

GenotypeQuality
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bin: 8.75e1
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
all individuals: 3157
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GenotypeQuality
all individuals: 1571
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66124
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.41e0

VQSLOD
type: SiteQuality
SIO_000300: -2.364e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.024e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.609482e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: -1.284e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQ
type: SiteQuality
SIO_000300: 5.797e1

GenotypeQuality
all individuals: 56
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GenotypeQuality
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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: 163
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 68
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GenotypeQuality
all individuals: 354
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GenotypeQuality
all individuals: 142
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GenotypeQuality
all individuals: 1536
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GenotypeQuality
all individuals: 927
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.744316194473592e-5
allele num: 11436
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65096
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12314
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: -1.22e0

QD
type: SiteQuality
SIO_000300: 7.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.214e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

DP
type: SiteQuality
SIO_000300: 1.562513e6

FS
type: SiteQuality
SIO_000300: 4.912e0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.93e-1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 3.75e1
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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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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: 4163
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11990
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.539219307966999e-5
allele num: 64968
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

DP
type: SiteQuality
SIO_000300: 1.5586e6

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.597e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.719e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 8.906305664410402e-5
allele num: 11228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 5.38e-1

DP
type: SiteQuality
SIO_000300: 1.546656e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.76e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

QD
type: SiteQuality
SIO_000300: 1.196e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.317917614354308e-5
allele num: 63312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11156
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.55e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

DP
type: SiteQuality
SIO_000300: 1.469147e6

FS
type: SiteQuality
SIO_000300: 4.458e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.869e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 5.001000200040008e-4
allele num: 9998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62884
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.496e0

MQRankSum
type: SiteQuality
SIO_000300: -1.95e-1

DP
type: SiteQuality
SIO_000300: 1.430413e6

QD
type: SiteQuality
SIO_000300: 1.409e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.595099853250813e-5
allele num: 62692
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.090988435522584e-4
allele num: 9166
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

FS
type: SiteQuality
SIO_000300: 1.158e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.27e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.41e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.94e0

DP
type: SiteQuality
SIO_000300: 1.420965e6

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9096
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.004621257785815e-4
allele num: 9954
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.66e-1

DP
type: SiteQuality
SIO_000300: 1.398513e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

VQSLOD
type: SiteQuality
SIO_000300: 3.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.438e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.404e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 362

Latino
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allele count: 9
allele frequency: 8.165487207403375e-4
allele num: 11022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 269
allele frequency: 4.305791209143004e-3
allele num: 62474
num of homozygotes: 3

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 5.029169181251257e-4
allele num: 9942
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8972
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 87
allele frequency: 1.339698182938097e-2
allele num: 6494
num of homozygotes: 3

Other
type: Population
allele count: 1
allele frequency: 1.295336787564767e-3
allele num: 772
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.548e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

FS
type: SiteQuality
SIO_000300: 7.99e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.99e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.383393e6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7974
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.476876421531463e-5
allele num: 10552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 736
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60096
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7774
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African
type: Population
allele count: 13
allele frequency: 1.351632355999168e-3
allele num: 9618
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

FS
type: SiteQuality
SIO_000300: 9.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -2.518e0

QD
type: SiteQuality
SIO_000300: 1.363e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-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
all individuals: 4630
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GenotypeQuality
all individuals: 6590
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.944444444444444e-5
allele num: 14400
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.577e0

MQRankSum
type: SiteQuality
SIO_000300: 1.48e-1

DP
type: SiteQuality
SIO_000300: 1.787249e6

VQSLOD
type: SiteQuality
SIO_000300: -9.066e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.845e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.87e-1

QD
type: SiteQuality
SIO_000300: 8.279999999999999e0

FS
type: SiteQuality
SIO_000300: 1.996e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

GenotypeQuality
all individuals: 735
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4648
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1935
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3609
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3200
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14466
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.165772907437631e-4
allele num: 8578
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.027e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.02e-2

FS
type: SiteQuality
SIO_000300: 3.612e0

MQ
type: SiteQuality
SIO_000300: 5.887e1

QD
type: SiteQuality
SIO_000300: 1.341e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.062e0

DP
type: SiteQuality
SIO_000300: 1.793269e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

GenotypeQuality
all individuals: 9410
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6600
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1939
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3635
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3208
bin: 8.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 66002
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 12
allele frequency: 1.394376016732512e-3
allele num: 8606
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14968
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.21e-1

DP
type: SiteQuality
SIO_000300: 1.814437e6

MQ
type: SiteQuality
SIO_000300: 5.567e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.31e0

FS
type: SiteQuality
SIO_000300: 2.619e0

MQRankSum
type: SiteQuality
SIO_000300: -1.349e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

QD
type: SiteQuality
SIO_000300: 1.292e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 27935
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9509
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4683
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3210
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1433
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15480
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510209012927389e-5
allele num: 66216
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.775e0

DP
type: SiteQuality
SIO_000300: 1.826732e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.083e1

MQRankSum
type: SiteQuality
SIO_000300: -8.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-1