http://identifiers.org/exac.variant/6-72968809-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968809
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968809
    reference: chr 6
allele count: 2
allele frequency: 1.685374321636835e-5
allele num: 118668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3369A>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1227A>C
  hgvsp: ENSP00000389503.2:p.Gln409His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1768A>C
  hgvsp: ENSP00000430359.1:p.Gln590His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1425A>C
  hgvsp: ENSP00000428367.1:p.Gln475His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3048A>C
  hgvsp: ENSP00000264839.7:p.Gln1016His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.723A>C
  hgvsp: ENSP00000359448.4:p.Gln241His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3048A>C
  hgvsp: ENSP00000428417.1:p.Gln1016His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3048A>C
  hgvsp: ENSP00000430101.1:p.Gln1016His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1227A>C
  hgvsp: ENSP00000411235.2:p.Gln409His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3045A>C
  hgvsp: ENSP00000275037.6:p.Gln1015His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1854A>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3045A>C
  hgvsp: ENSP00000430932.1:p.Gln1015His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.320A>C
  hgvsp: ENSP00000429338.1:p.Gln107His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-16A>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3048A>C
  hgvsp: ENSP00000430408.1:p.Gln1016His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3045A>C
  hgvsp: ENSP00000430502.1:p.Gln1015His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1470A>C
  hgvsp: ENSP00000428328.1:p.Gln490His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1467A>C
  hgvsp: ENSP00000385649.3:p.Gln489His
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3045A>C
  hgvsp: ENSP00000429959.1:p.Gln1015His
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln1016His
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

6-72968816-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968816
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968816
    reference: chr 6
allele count: 1
allele frequency: 8.530094172239662e-6
allele num: 117232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+2T>C
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1535
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3053+2T>C
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: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

6-72968829-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968829
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968829
    reference: chr 6
allele count: 1
allele frequency: 8.748906386701662e-6
allele num: 114300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+15T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+15T>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7793
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

6-72968833-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968833
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968833
    reference: chr 6
allele count: 2
allele frequency: 1.767658912536237e-5
allele num: 113144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+19A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+19A>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11257
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/6-72968835-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968835
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968835
    reference: chr 6
allele count: 15
allele frequency: 1.335089718029052e-4
allele num: 112352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+21C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+21C>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

6-72968837-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968837
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968837
    reference: chr 6
allele count: 15
allele frequency: 1.341105786424433e-4
allele num: 111848
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+23C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+23C>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7245
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

6-72968837-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968837
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968837
    reference: chr 6
allele count: 2
allele frequency: 1.788141048565911e-5
allele num: 111848
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+23C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+23C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7245
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

6-72968840-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968840
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968840
    reference: chr 6
allele count: 17
allele frequency: 1.529134509867415e-4
allele num: 111174
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+26C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+26C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

6-72968841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968841
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968841
    reference: chr 6
allele count: 3
allele frequency: 2.704749540192578e-5
allele num: 110916
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+27G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+27G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16077
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum

6-72968845-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968845
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968845
    reference: chr 6
allele count: 2
allele frequency: 1.818743975410581e-5
allele num: 109966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+31T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+31T>C
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4383
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

6-72968858-CTGTTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968858
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968853
    reference: chr 6
allele count: 1
allele frequency: 9.619269320302431e-6
allele num: 103958
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+46_1475+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+46_325+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+46_728+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+46_-11+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+46_3053+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+46_3374+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+46_3050+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+46_1232+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+46_3053+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+46_1430+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+46_3050+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+46_1859+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+46_1472+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+46_1773+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+46_1232+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+46_3050+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+46_3050+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+46_3053+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+46_3053+50delGTTTT
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: CTGTTT
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-72968861-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72968861
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72968861
    reference: chr 6
allele count: 1
allele frequency: 9.775553296316572e-6
allele num: 102296
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3374+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3053+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3053+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1859+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3053+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-11+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3050+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.728+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3050+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1232+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1472+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3050+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1430+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3053+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.325+47T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1475+47T>C
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-72970358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970358
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970358
    reference: chr 6
allele count: 3
allele frequency: 2.808988764044944e-5
allele num: 106800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3375-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1473-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3054-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1431-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3054-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1544C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1544C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1476-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3051-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-10-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3054-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3054-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1860-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3051-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1544C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.326-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1233-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.729-50C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3051-50C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-72970365-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970365
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970365
    reference: chr 6
allele count: 2
allele frequency: 1.865880509012203e-5
allele num: 107188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-10-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1860-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3054-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1551C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3051-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1431-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.729-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1473-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3054-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1476-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.326-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3375-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3051-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3054-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1551C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3054-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1233-43C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1551C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3051-43C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10928
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

6-72970366-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970366
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970366
    reference: chr 6
allele count: 3
allele frequency: 2.793348107041099e-5
allele num: 107398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3375-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1431-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3054-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3051-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3054-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3051-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-10-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3051-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3054-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1552A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1233-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1552A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1860-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.729-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1552A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1473-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.326-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1476-42A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3054-42A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

6-72970392-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970392
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970392
    reference: chr 6
allele count: 3
allele frequency: 2.691403656720435e-5
allele num: 111466
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3054-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3054-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1473-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1860-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1578C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3051-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3375-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-10-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1431-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1578C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3054-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1578C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.326-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3051-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3054-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3051-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1476-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1233-16C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.729-16C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

6-72970393-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970393
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970393
    reference: chr 6
allele count: 1
allele frequency: 8.949186518945427e-6
allele num: 111742
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-10-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.729-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3051-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1579A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.326-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3054-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3051-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1476-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1233-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1431-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1579A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3375-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3054-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3051-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3054-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1860-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1579A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3054-15A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1473-15A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

6-72970398-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970398
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970398
    reference: chr 6
allele count: 1
allele frequency: 8.879417510211331e-6
allele num: 112620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1584G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3375-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1584G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1860-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1431-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3051-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3054-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3054-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.729-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1584G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3054-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1233-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.326-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3054-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1476-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3051-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3051-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-10-10G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1473-10G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7005
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

6-72970400-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970400
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970400
    reference: chr 6
allele count: 1
allele frequency: 8.854102105505481e-6
allele num: 112942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1473-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1431-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3375-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3054-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3051-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3054-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3051-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1233-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3051-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3054-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1586C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1476-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-10-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1860-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.729-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.326-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3054-8C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1586C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1586C>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.3054-8C>G
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

6-72970416-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970416
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970416
    reference: chr 6
allele count: 3
allele frequency: 2.614470221184181e-5
allele num: 114746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3062T>C
  hgvsp: ENSP00000264839.7:p.Leu1021Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1602T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3062T>C
  hgvsp: ENSP00000430101.1:p.Leu1021Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1602T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.737T>C
  hgvsp: ENSP00000359448.4:p.Leu246Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.334T>C
  hgvsp: ENSP00000429338.1:p.Leu112Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1481T>C
  hgvsp: ENSP00000385649.3:p.Leu494Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1868T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3059T>C
  hgvsp: ENSP00000275037.6:p.Leu1020Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3062T>C
  hgvsp: ENSP00000428417.1:p.Leu1021Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.-2T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1484T>C
  hgvsp: ENSP00000428328.1:p.Leu495Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1241T>C
  hgvsp: ENSP00000411235.2:p.Leu414Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3059T>C
  hgvsp: ENSP00000429959.1:p.Leu1020Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3062T>C
  hgvsp: ENSP00000430408.1:p.Leu1021Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3059T>C
  hgvsp: ENSP00000430502.1:p.Leu1020Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.15T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3383T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1602T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1439T>C
  hgvsp: ENSP00000428367.1:p.Leu480Pro
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu1021Pro
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum

6-72970418-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970418
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970418
    reference: chr 6
allele count: 3
allele frequency: 2.610284521012791e-5
allele num: 114930
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3064A>G
  hgvsp: ENSP00000428417.1:p.Met1022Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3064A>G
  hgvsp: ENSP00000264839.7:p.Met1022Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1483A>G
  hgvsp: ENSP00000385649.3:p.Met495Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3061A>G
  hgvsp: ENSP00000430502.1:p.Met1021Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1243A>G
  hgvsp: ENSP00000411235.2:p.Met415Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.739A>G
  hgvsp: ENSP00000359448.4:p.Met247Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3061A>G
  hgvsp: ENSP00000275037.6:p.Met1021Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.1A>G
  hgvsp: ENSP00000439730.1:p.Met1?
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.336A>G
  hgvsp: ENSP00000429338.1:p.Met113Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3064A>G
  hgvsp: ENSP00000430408.1:p.Met1022Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3061A>G
  hgvsp: ENSP00000429959.1:p.Met1021Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.17A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3064A>G
  hgvsp: ENSP00000430101.1:p.Met1022Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1441A>G
  hgvsp: ENSP00000428367.1:p.Met481Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1604A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3385A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1486A>G
  hgvsp: ENSP00000428328.1:p.Met496Val
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1604A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1870A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1604A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD

6-72970423-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970423
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970423
    reference: chr 6
allele count: 2
allele frequency: 1.736442723436767e-5
allele num: 115178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1875G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.341G>T
  hgvsp: ENST00000522211.1:c.341G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1609G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3069G>T
  hgvsp: ENST00000521978.1:c.3069G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3066G>T
  hgvsp: ENST00000348717.5:c.3066G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1248G>T
  hgvsp: ENST00000425662.2:c.1248G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3066G>T
  hgvsp: ENST00000520567.1:c.3066G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.6G>T
  hgvsp: ENST00000538414.1:c.6G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1446G>T
  hgvsp: ENST00000517827.1:c.1446G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.744G>T
  hgvsp: ENST00000370420.4:c.744G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3069G>T
  hgvsp: ENST00000264839.7:c.3069G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1488G>T
  hgvsp: ENST00000401910.3:c.1488G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1609G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3390G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.22G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1609G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1491G>T
  hgvsp: ENST00000523963.1:c.1491G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3069G>T
  hgvsp: ENST00000518273.1:c.3069G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3066G>T
  hgvsp: ENST00000517960.1:c.3066G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3069G>T
  hgvsp: ENST00000491071.2:c.3069G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu1023Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

6-72970436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970436
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970436
    reference: chr 6
allele count: 1
allele frequency: 8.668515950069348e-6
allele num: 115360
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1501C>T
  hgvsp: ENSP00000385649.3:p.Arg501Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.354C>T
  hgvsp: ENSP00000429338.1:p.Arg119Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3082C>T
  hgvsp: ENSP00000430101.1:p.Arg1028Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3079C>T
  hgvsp: ENSP00000275037.6:p.Arg1027Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3079C>T
  hgvsp: ENSP00000429959.1:p.Arg1027Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3082C>T
  hgvsp: ENSP00000428417.1:p.Arg1028Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.35C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1622C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.19C>T
  hgvsp: ENSP00000439730.1:p.Arg7Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3082C>T
  hgvsp: ENSP00000264839.7:p.Arg1028Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3082C>T
  hgvsp: ENSP00000430408.1:p.Arg1028Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1459C>T
  hgvsp: ENSP00000428367.1:p.Arg487Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1261C>T
  hgvsp: ENSP00000411235.2:p.Arg421Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3403C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.757C>T
  hgvsp: ENSP00000359448.4:p.Arg253Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3079C>T
  hgvsp: ENSP00000430502.1:p.Arg1027Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1622C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1622C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1888C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1504C>T
  hgvsp: ENSP00000428328.1:p.Arg502Ter
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg1028Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

6-72970443-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970443
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970443
    reference: chr 6
allele count: 4
allele frequency: 3.477293274914807e-5
allele num: 115032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1511G>A
  hgvsp: ENSP00000428328.1:p.Arg504Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3086G>A
  hgvsp: ENSP00000430502.1:p.Arg1029Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1895G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1268G>A
  hgvsp: ENSP00000411235.2:p.Arg423Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3089G>A
  hgvsp: ENSP00000428417.1:p.Arg1030Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3086G>A
  hgvsp: ENSP00000275037.6:p.Arg1029Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3089G>A
  hgvsp: ENSP00000264839.7:p.Arg1030Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.764G>A
  hgvsp: ENSP00000359448.4:p.Arg255Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3089G>A
  hgvsp: ENSP00000430101.1:p.Arg1030Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3086G>A
  hgvsp: ENSP00000429959.1:p.Arg1029Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1629G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3410G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1466G>A
  hgvsp: ENSP00000428367.1:p.Arg489Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1629G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.361G>A
  hgvsp: ENSP00000429338.1:p.Arg121Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1508G>A
  hgvsp: ENSP00000385649.3:p.Arg503Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3089G>A
  hgvsp: ENSP00000430408.1:p.Arg1030Gln
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1629G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.42G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.26G>A
  hgvsp: ENSP00000439730.1:p.Arg9Gln
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg1030Gln
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

6-72970466-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970466
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970466
    reference: chr 6
allele count: 3
allele frequency: 2.666761484852795e-5
allele num: 112496
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1489A>G
  hgvsp: ENSP00000428367.1:p.Thr497Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1534A>G
  hgvsp: ENSP00000428328.1:p.Thr512Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1531A>G
  hgvsp: ENSP00000385649.3:p.Thr511Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.65A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3109A>G
  hgvsp: ENSP00000430502.1:p.Thr1037Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3109A>G
  hgvsp: ENSP00000429959.1:p.Thr1037Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1291A>G
  hgvsp: ENSP00000411235.2:p.Thr431Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3112A>G
  hgvsp: ENSP00000428417.1:p.Thr1038Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3112A>G
  hgvsp: ENSP00000264839.7:p.Thr1038Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1652A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.384A>G
  hgvsp: ENSP00000429338.1:p.Thr129Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.49A>G
  hgvsp: ENSP00000439730.1:p.Thr17Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.787A>G
  hgvsp: ENSP00000359448.4:p.Thr263Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3109A>G
  hgvsp: ENSP00000275037.6:p.Thr1037Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3112A>G
  hgvsp: ENSP00000430101.1:p.Thr1038Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1652A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3112A>G
  hgvsp: ENSP00000430408.1:p.Thr1038Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3433A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1652A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr1038Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/6-72970468-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970468
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970468
    reference: chr 6
allele count: 5
allele frequency: 4.485028973287167e-5
allele num: 111482
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1920C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.789C>A
  hgvsp: ENST00000370420.4:c.789C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3114C>A
  hgvsp: ENST00000518273.1:c.3114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1533C>A
  hgvsp: ENST00000401910.3:c.1533C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3114C>A
  hgvsp: ENST00000264839.7:c.3114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.51C>A
  hgvsp: ENST00000538414.1:c.51C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3114C>A
  hgvsp: ENST00000491071.2:c.3114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3111C>A
  hgvsp: ENST00000520567.1:c.3111C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1654C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1491C>A
  hgvsp: ENST00000517827.1:c.1491C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1654C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.67C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.386C>A
  hgvsp: ENST00000522211.1:c.386C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3111C>A
  hgvsp: ENST00000348717.5:c.3111C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3114C>A
  hgvsp: ENST00000521978.1:c.3114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3435C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1536C>A
  hgvsp: ENST00000523963.1:c.1536C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1654C>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.3114C>A
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

6-72970479-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970479
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970479
    reference: chr 6
allele count: 1
allele frequency: 9.067662900564009e-6
allele num: 110282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1665A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3446A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1665A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+9A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1665A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-72970482-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970482
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970482
    reference: chr 6
allele count: 2
allele frequency: 1.821858660205141e-5
allele num: 109778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3449G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1668G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1668G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1668G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+12G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+12G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

6-72970487-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970487
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970487
    reference: chr 6
allele count: 1
allele frequency: 9.191683364891447e-6
allele num: 108794
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1673G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3454G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1673G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1673G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+17G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+17G>C
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17628
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

6-72970488-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970488
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970488
    reference: chr 6
allele count: 1
allele frequency: 9.199970560094207e-6
allele num: 108696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1674G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1674G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3455G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1674G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+18G>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+18G>C
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

6-72970493-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970493
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970493
    reference: chr 6
allele count: 1
allele frequency: 9.269386922748929e-6
allele num: 107882
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1679G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1679G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3460G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1679G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+23G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

6-72970494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970494
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970494
    reference: chr 6
allele count: 1
allele frequency: 9.325226603006453e-6
allele num: 107236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3461G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1680G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1680G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1680G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+24G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+24G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

6-72970498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970498
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970498
    reference: chr 6
allele count: 1
allele frequency: 9.360140776517278e-6
allele num: 106836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1684C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1684C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3465C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1684C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+28C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+28C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-72970504-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970504
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970504
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 105692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1690G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1690G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1690G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3471G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+34G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+34G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

6-72970510-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970510
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970510
    reference: chr 6
allele count: 1
allele frequency: 9.642829591915451e-6
allele num: 103704
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3477A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1696A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1696A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1696A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+40A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+40A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12425
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

6-72970518-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970518
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970518
    reference: chr 6
allele count: 1
allele frequency: 9.957977335643584e-6
allele num: 100422
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1704T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1704T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3485T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1704T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+48T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+48T>C
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

6-72970521-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970521
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970521
    reference: chr 6
allele count: 1
allele frequency: 1.021617424706796e-5
allele num: 97884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1707A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1707A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1707A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3488A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+51A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+51A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9134
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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: A
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

6-72970522-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72970522
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72970522
    reference: chr 6
allele count: 4
allele frequency: 4.082382478414402e-5
allele num: 97982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1493+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1535+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3116+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+1708T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000370419
  gene symbol: RIMS1
  hgvsc: ENST00000370419.2:n.3489T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3113+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3116+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+1708T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1295+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3116+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1922+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3116+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+1708T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.791+52T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1538+52T>C
  variant of: http://identifiers.org/hgnc/17282
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-72974654-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974654
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974654
    reference: chr 6
allele count: 2
allele frequency: 5.958765343820761e-5
allele num: 33564
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5840C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4184C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4184C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-1009C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5840C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-1009C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-1009C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-24C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4184C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-1009C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-24C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4184C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-1009C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5840C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-1009C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-1009C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4184C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-1009C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-1009C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

6-72974655-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974655
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974655
    reference: chr 6
allele count: 3
allele frequency: 8.712825278810409e-5
allele num: 34432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4185G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5841G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4185G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4185G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5841G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5841G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-23G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4185G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-1008G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4185G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

6-72974661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974661
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974661
    reference: chr 6
allele count: 1
allele frequency: 2.734332276058187e-5
allele num: 36572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-17G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5847G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4191G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5847G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-17G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4191G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4191G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4191G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-1002G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5847G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4191G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33995
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-72974663-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974663
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974663
    reference: chr 6
allele count: 1
allele frequency: 2.685573101299817e-5
allele num: 37236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5849G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-15G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5849G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4193G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4193G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4193G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4193G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-1000G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5849G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4193G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-15G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

6-72974670-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974670
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974670
    reference: chr 6
allele count: 1
allele frequency: 2.524487529031606e-5
allele num: 39612
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-8C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-993C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5856C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-993C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-993C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-993C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4200C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-8C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4200C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-993C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5856C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5856C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4200C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4200C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-993C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-993C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4200C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-993C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-993C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3117-8C>T
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

6-72974670-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974670
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974669
    reference: chr 6
allele count: 1
allele frequency: 2.524487529031606e-5
allele num: 39612
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4201delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5857delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-7delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4201delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4201delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5857delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-7delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4201delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5857delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-992delG
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4201delG
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3117-7delG
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: CG
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

6-72974671-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974671
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974671
    reference: chr 6
allele count: 8
allele frequency: 1.993223041658362e-4
allele num: 40136
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5857G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4201G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4201G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-992G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5857G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-992G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-992G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4201G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-7G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-992G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-992G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-7G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4201G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-992G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-992G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4201G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5857G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-992G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-992G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6310
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.3117-7G>A
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

6-72974671-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974671
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974671
    reference: chr 6
allele count: 1
allele frequency: 2.491528802072952e-5
allele num: 40136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-992G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-992G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-7G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-992G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-992G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4201G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5857G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-7G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-992G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4201G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4201G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4201G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-992G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5857G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5857G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-992G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-992G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4201G>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-992G>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3117-7G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-72974674-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974674
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974674
    reference: chr 6
allele count: 1
allele frequency: 2.428363283147159e-5
allele num: 41180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-989C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-989C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3117-4C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-989C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-989C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5860C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5860C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-989C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4204C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-989C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4204C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3117-4C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-989C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4204C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-989C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4204C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5860C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4204C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-989C>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3117-4C>G
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: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

6-72974683-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974683
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974683
    reference: chr 6
allele count: 16
allele frequency: 3.506311360448808e-4
allele num: 45632
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5869T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5869T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3122T>C
  hgvsp: ENSP00000264839.7:p.Leu1041Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5869T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4213T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4213T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3122T>C
  hgvsp: ENSP00000428417.1:p.Leu1041Pro
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-980T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4213T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4213T>C
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4213T>C
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1041Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

6-72974696-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974696
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974695
    reference: chr 6
allele count: 25
allele frequency: 4.933885928557331e-4
allele num: 50670
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3139delA
  hgvsp: ENSP00000428417.1:p.Thr1047HisfsTer31
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-963delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-963delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-963delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3139delA
  hgvsp: ENSP00000264839.7:p.Thr1047HisfsTer36
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-963delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-963delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-963delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5886delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4230delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4230delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5886delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4230delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4230delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-963delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5886delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4230delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-963delA
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-963delA
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3595
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Thr1047HisfsTer31
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: TA
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-72974700-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974700
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974700
    reference: chr 6
allele count: 1
allele frequency: 1.929458979702092e-5
allele num: 51828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4230A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4230A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5886A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-963A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4230A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-963A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-963A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3139A>G
  hgvsp: ENSP00000264839.7:p.Thr1047Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5886A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-963A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5886A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-963A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-963A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4230A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-963A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4230A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3139A>G
  hgvsp: ENSP00000428417.1:p.Thr1047Ala
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-963A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-963A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1047Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

6-72974700-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974700
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974700
    reference: chr 6
allele count: 2
allele frequency: 3.858917959404183e-5
allele num: 51828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4230A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5886A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5886A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4230A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5886A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4230A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3139A>T
  hgvsp: ENSP00000264839.7:p.Thr1047Ser
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4230A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4230A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-963A>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3139A>T
  hgvsp: ENSP00000428417.1:p.Thr1047Ser
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1047Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

6-72974706-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974706
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974706
    reference: chr 6
allele count: 2
allele frequency: 3.807928106317353e-5
allele num: 52522
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3145C>T
  hgvsp: ENSP00000428417.1:p.Pro1049Ser
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-957C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-957C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4236C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-957C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3145C>T
  hgvsp: ENSP00000264839.7:p.Pro1049Ser
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-957C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4236C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-957C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5892C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5892C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4236C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4236C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4236C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5892C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-957C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-957C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-957C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-957C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro1049Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

6-72974714-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974714
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974714
    reference: chr 6
allele count: 1
allele frequency: 1.878710453144961e-5
allele num: 53228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4244G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4244G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4244G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5900G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3153G>A
  hgvsp: ENST00000264839.7:c.3153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3153G>A
  hgvsp: ENST00000521978.1:c.3153G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5900G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4244G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4244G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-949G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5900G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys1051Lys
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

6-72974722-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974722
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974722
    reference: chr 6
allele count: 1
allele frequency: 1.903891554337065e-5
allele num: 52524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5908T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3161T>G
  hgvsp: ENSP00000264839.7:p.Leu1054Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3161T>G
  hgvsp: ENSP00000428417.1:p.Leu1054Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4252T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4252T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4252T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5908T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4252T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-941T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4252T>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5908T>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu1054Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

6-72974732-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974732
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974732
    reference: chr 6
allele count: 43
allele frequency: 8.285802373978727e-4
allele num: 51896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5918C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3171C>T
  hgvsp: ENST00000264839.7:c.3171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-931C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-931C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4262C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4262C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-931C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-931C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3171C>T
  hgvsp: ENST00000521978.1:c.3171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5918C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4262C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-931C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4262C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-931C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-931C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5918C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4262C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-931C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-931C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8000
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3984
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser1057Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

6-72974739-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974739
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974739
    reference: chr 6
allele count: 1
allele frequency: 1.94265288678219e-5
allele num: 51476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3178C>T
  hgvsp: ENSP00000264839.7:p.His1060Tyr
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4269C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4269C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4269C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5925C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4269C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5925C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3178C>T
  hgvsp: ENSP00000428417.1:p.His1060Tyr
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-924C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4269C>T
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5925C>T
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His1060Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum

6-72974740-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974740
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974740
    reference: chr 6
allele count: 1
allele frequency: 1.943710153941844e-5
allele num: 51448
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3179A>G
  hgvsp: ENSP00000428417.1:p.His1060Arg
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4270A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-923A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4270A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-923A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5926A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3179A>G
  hgvsp: ENSP00000264839.7:p.His1060Arg
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-923A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-923A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5926A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-923A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5926A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4270A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-923A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-923A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4270A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-923A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4270A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-923A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His1060Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

6-72974743-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974743
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974743
    reference: chr 6
allele count: 3
allele frequency: 5.880047040376323e-5
allele num: 51020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4273G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5929G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4273G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4273G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3182G>A
  hgvsp: ENSP00000428417.1:p.Trp1061Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5929G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4273G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3182G>A
  hgvsp: ENSP00000264839.7:p.Trp1061Ter
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5929G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-920G>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4273G>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Trp1061Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

6-72974745-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974745
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974745
    reference: chr 6
allele count: 3
allele frequency: 5.89622641509434e-5
allele num: 50880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3184A>G
  hgvsp: ENSP00000428417.1:p.Asn1062Asp
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4275A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5931A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5931A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5931A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4275A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4275A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3184A>G
  hgvsp: ENSP00000264839.7:p.Asn1062Asp
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4275A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4275A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-918A>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-918A>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn1062Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/6-72974764-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974764
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974764
    reference: chr 6
allele count: 24
allele frequency: 5.15331100231899e-4
allele num: 46572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-899C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4294C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-899C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-899C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5950C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5950C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4294C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-899C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4294C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4294C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4294C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-899C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3194+9C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-899C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-899C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3194+9C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-899C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5950C>A
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-899C>A
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

6-72974769-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 72974769
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 72974769
    reference: chr 6
allele count: 2
allele frequency: 4.469473496022169e-5
allele num: 44748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000389503
  ensembl transcript: ENST00000453976
  gene symbol: RIMS1
  hgvsc: ENST00000453976.2:c.1232+5955C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430502
  ensembl transcript: ENST00000520567
  gene symbol: RIMS1
  hgvsc: ENST00000520567.1:c.3114-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429338
  ensembl transcript: ENST00000522211
  gene symbol: RIMS1
  hgvsc: ENST00000522211.1:c.388+4299C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428367
  ensembl transcript: ENST00000517827
  gene symbol: RIMS1
  hgvsc: ENST00000517827.1:c.1494-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428417
  ensembl transcript: ENST00000521978
  gene symbol: RIMS1
  hgvsc: ENST00000521978.1:c.3194+14C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430408
  ensembl transcript: ENST00000518273
  gene symbol: RIMS1
  hgvsc: ENST00000518273.1:c.3117-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000439730
  ensembl transcript: ENST00000538414
  gene symbol: RIMS1
  hgvsc: ENST00000538414.1:c.53+4299C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430101
  ensembl transcript: ENST00000491071
  gene symbol: RIMS1
  hgvsc: ENST00000491071.2:c.3117-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000428328
  ensembl transcript: ENST00000523963
  gene symbol: RIMS1
  hgvsc: ENST00000523963.1:c.1539-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000411235
  ensembl transcript: ENST00000425662
  gene symbol: RIMS1
  hgvsc: ENST00000425662.2:c.1296-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430932
  ensembl transcript: ENST00000522291
  gene symbol: RIMS1
  hgvsc: ENST00000522291.1:c.3050+5955C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000275037
  ensembl transcript: ENST00000348717
  gene symbol: RIMS1
  hgvsc: ENST00000348717.5:c.3113+4299C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000264839
  ensembl transcript: ENST00000264839
  gene symbol: RIMS1
  hgvsc: ENST00000264839.7:c.3194+14C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000430359
  ensembl transcript: ENST00000517433
  gene symbol: RIMS1
  hgvsc: ENST00000517433.1:c.1773+5955C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000359448
  ensembl transcript: ENST00000370420
  gene symbol: RIMS1
  hgvsc: ENST00000370420.4:c.792-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000429959
  ensembl transcript: ENST00000517960
  gene symbol: RIMS1
  hgvsc: ENST00000517960.1:c.3113+4299C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl protein: ENSP00000385649
  ensembl transcript: ENST00000401910
  gene symbol: RIMS1
  hgvsc: ENST00000401910.3:c.1536-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000524197
  gene symbol: RIMS1
  hgvsc: ENST00000524197.1:n.1923-894C>G
  variant of: http://identifiers.org/hgnc/17282
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000079841
  ensembl transcript: ENST00000463023
  gene symbol: RIMS1
  hgvsc: ENST00000463023.2:n.69+4299C>G
  variant of: http://identifiers.org/hgnc/17282
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 9843
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 304
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 210
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12078
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 341
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1440
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 429
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 823
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 151
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 940
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29553
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 78
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2061
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 236
bin: 6.25e1
variant carriers: 0

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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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QD
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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African
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East Asian
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South Asian
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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East Asian
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Other
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Latino
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FS
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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South Asian
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Other
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MQ
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BaseQRankSum
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FS
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DP
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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Latino
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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FS
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 16

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

East Asian
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allele count: 15
allele frequency: 1.94300518134715e-3
allele num: 7720
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61380
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

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

FS
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ClippingRankSum
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SIO_000300: -3.61e-1

BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 7.5e-2

QD
type: SiteQuality
SIO_000300: 1.741e1

DP
type: SiteQuality
SIO_000300: 1.477815e6

GenotypeDepth
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bin: 7.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9336
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7720
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.258390355164549e-5
allele num: 61380
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
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SIO_000300: 0.0e0

MQ
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SIO_000300: 6.0e1

QD
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: 3.2e-3

BaseQRankSum
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SIO_000300: -9.22e-1

MQRankSum
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SIO_000300: -4.29e-1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 17

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

European (Non-Finnish)
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allele count: 16
allele frequency: 2.623638987275351e-4
allele num: 60984
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9298
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.366182836771072e-5
allele num: 15708
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7640
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.19e-1

ReadPosRankSum
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SIO_000300: -5.34e-1

ClippingRankSum
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InbreedingCoeff
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SIO_000300: 3.9e-3

DP
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FS
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SIO_000300: 4.28e0

BaseQRankSum
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QD
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SIO_000300: 1.254e1

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.366182836771072e-5
allele num: 15708
num of homozygotes: 0

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

Latino
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allele frequency: 1.95579894386857e-4
allele num: 10226
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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QD
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VQSLOD
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DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.322259136212625e-5
allele num: 60200
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African
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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num of homozygotes: 0

East Asian
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Latino
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InbreedingCoeff
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DP
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
type: Population
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South Asian
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DP
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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East Asian
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South Asian
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FS
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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FS
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MQ
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VQSLOD
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QD
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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FS
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VQSLOD
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QD
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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South Asian
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African
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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MQ
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FS
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VQSLOD
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DP
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GenotypeQuality
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Latino
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South Asian
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European (Non-Finnish)
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African
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East Asian
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VQSLOD
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QD
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MQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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European (Finnish)
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FS
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BaseQRankSum
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QD
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DP
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MQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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Latino
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DP
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QD
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MQ
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FS
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MQRankSum
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Latino
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African
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European (Non-Finnish)
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MQ
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MQRankSum
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VQSLOD
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FS
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DP
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QD
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ReadPosRankSum
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European (Finnish)
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European (Non-Finnish)
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South Asian
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African
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East Asian
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MQ
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DP
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VQSLOD
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QD
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GenotypeDepth
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bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 719
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 804
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32750
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 556
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1591
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8591
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 720
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 766
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3668
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 685
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11243
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3356
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 414
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.391772303276728e-4
allele num: 8362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10862
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9212
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.734e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-1

FS
type: SiteQuality
SIO_000300: 1.1644e1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

DP
type: SiteQuality
SIO_000300: 2.127131e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.287e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

QD
type: SiteQuality
SIO_000300: 6.85e0

MQ
type: SiteQuality
SIO_000300: 5.82e1

GenotypeDepth
all individuals: 766
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1579
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 721
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2562
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9088
bin: 2.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 721
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 32173
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 719
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2066
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 808
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 714
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 681
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 556
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3668
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3528
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37366
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2876
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11240
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 564
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64246
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9240
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.549646319098769e-5
allele num: 15268
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

QD
type: SiteQuality
SIO_000300: 1.833e1

FS
type: SiteQuality
SIO_000300: 1.596e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.073e0

DP
type: SiteQuality
SIO_000300: 2.129907e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

GenotypeDepth
all individuals: 2498
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 719
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3669
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 9280
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 715
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 556
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 931
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 736
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2715
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 31252
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 765
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1581
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3931
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2819
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11242
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 36444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.171081198436822e-4
allele num: 9212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15196
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.121001217190475e-5
allele num: 64082
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.76e-1

FS
type: SiteQuality
SIO_000300: 1.095e0

QD
type: SiteQuality
SIO_000300: 1.129e1

DP
type: SiteQuality
SIO_000300: 2.124935e6

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-2

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeDepth
all individuals: 716
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 720
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 26850
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 719
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8842
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1607
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1452
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 765
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5564
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 714
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3913
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 556
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3669
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 745
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1477
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6802
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2550
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 587
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32167
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11242
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14912
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.792944785276074e-5
allele num: 62592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9062
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.68e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

QD
type: SiteQuality
SIO_000300: 1.332e1

DP
type: SiteQuality
SIO_000300: 2.070949e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000079841
ensembl protein: ENSP00000411235
ensembl transcript: ENST00000425662
gene symbol: RIMS1
hgvsc: ENST00000425662.2:c.1293C>A
hgvsp: ENST00000425662.2:c.1293C>A(p.%3D)
variant of: http://identifiers.org/hgnc/17282

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000079841
ensembl protein: ENSP00000429959
ensembl transcript: ENST00000517960
gene symbol: RIMS1
hgvsc: ENST00000517960.1:c.3111C>A
hgvsp: ENST00000517960.1:c.3111C>A(p.%3D)
variant of: http://identifiers.org/hgnc/17282

GenotypeDepth
all individuals: 702
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24736
bin: 2.25e1
variant carriers: 2

GenotypeDepth
all individuals: 745
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4309
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 734
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8672
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6945
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3669
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 682
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 724
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 281
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 765
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 619
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1494
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 650
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 719
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 723
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 714
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 556
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2022
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2243
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7876
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1410
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1896
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 549
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11243
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28432
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 515
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 4
allele frequency: 3.84172109104879e-4
allele num: 10412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9040
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.612435099487246e-5
allele num: 62018
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

FS
type: SiteQuality
SIO_000300: 1.451e0

VQSLOD
type: SiteQuality
SIO_000300: -1.986e-1

MQ
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DP
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QD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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South Asian
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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Other
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South Asian
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African
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East Asian
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ReadPosRankSum
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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East Asian
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FS
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MQ
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VQSLOD
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DP
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East Asian
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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InbreedingCoeff
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MQ
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FS
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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East Asian
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South Asian
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FS
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MQ
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VQSLOD
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DP
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QD
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GenotypeQuality
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African
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European (Finnish)
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FS
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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VQSLOD
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MQ
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ReadPosRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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VQSLOD
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MQRankSum
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FS
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MQ
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QD
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DP
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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South Asian
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MQ
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ReadPosRankSum
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MQRankSum
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FS
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VQSLOD
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QD
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DP
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East Asian
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Latino
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European (Finnish)
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MQ
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DP
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VQSLOD
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QD
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DP
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East Asian
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European (Non-Finnish)
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African
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African
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DP
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MQ
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European (Finnish)
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African
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FS
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African
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European (Non-Finnish)
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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East Asian
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Other
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South Asian
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Latino
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African
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European (Non-Finnish)
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Latino
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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MQ
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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East Asian
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South Asian
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VQSLOD
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DP
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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African
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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South Asian
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European (Finnish)
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East Asian
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FS
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QD
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MQRankSum
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MQ
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DP
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 1.128923007450892e-4
allele num: 8858
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2166
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 20096
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2652
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.86e0

DP
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SIO_000300: 9.67567e5

InbreedingCoeff
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SIO_000300: -1.09e-2

ClippingRankSum
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SIO_000300: -2.132e0

ReadPosRankSum
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SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 7.249e0

MQRankSum
type: SiteQuality
SIO_000300: -6.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.328e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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bin: 1.25e1
variant carriers: 7

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 1

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3174
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 3.408316291751875e-4
allele num: 2934
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 2672
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 6.653655074520937e-4
allele num: 22544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

BaseQRankSum
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SIO_000300: 0.0e0

FS
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SIO_000300: 1.974e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.003752e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

MQRankSum
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SIO_000300: 2.48e-1

QD
type: SiteQuality
SIO_000300: 1.63e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 4

GenotypeDepth
all individuals: 229
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 11

GenotypeDepth
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 22

GenotypeQuality
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GenotypeQuality
all individuals: 1084
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5268
num of homozygotes: 0

East Asian
type: Population
allele count: 25
allele frequency: 6.709608158883522e-3
allele num: 3726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.94e-1

DP
type: SiteQuality
SIO_000300: 1.045155e6

VQSLOD
type: SiteQuality
SIO_000300: 6.38e0

MQRankSum
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SIO_000300: 1.94e-1

QD
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SIO_000300: 1.195e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25854
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.047339757017176e-4
allele num: 9548
num of homozygotes: 0

Latino
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: 418
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 6.6e-3

DP
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: -4.8e-1

MQRankSum
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QD
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SIO_000300: 1.166e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3516
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 2.094679514034353e-4
allele num: 9548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 25854
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
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allele count: 0
allele frequency: 0.0e0
allele num: 5452
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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Other
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Latino
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allele frequency: 5.527915975677169e-4
allele num: 3618
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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num of homozygotes: 0

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

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

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

Latino
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allele num: 3600
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

FS
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SIO_000300: 0.0e0

BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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DP
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GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

East Asian
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African
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allele frequency: 6.902985074626866e-3
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European (Non-Finnish)
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Other
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South Asian
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Latino
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BaseQRankSum
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SIO_000300: -1.25e0

MQRankSum
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FS
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VQSLOD
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MQ
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 3418
num of homozygotes: 0

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

European (Non-Finnish)
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East Asian
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Latino
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South Asian
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Other
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European (Finnish)
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MQ
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -9.389999999999999e-1

GenotypeDepth
all individuals: 949
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 882
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 985
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7064
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 519
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1093
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1137
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4730
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 29711
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 228
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 135
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1046
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 710
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7029
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 32789
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 275
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 8046
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 670
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4793
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 448
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5646
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 197
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3756
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.787878787878788e-4
allele num: 5280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.923414940364093e-5
allele num: 25488
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

FS
type: SiteQuality
SIO_000300: 2.605e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.879e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

MQ
type: SiteQuality
SIO_000300: 5.916e1

DP
type: SiteQuality
SIO_000300: 1.010525e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.92e-1

QD
type: SiteQuality
SIO_000300: 2.725e1

GenotypeDepth
all individuals: 1047
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 315
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 518
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1065
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 984
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29671
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 4963
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6761
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7263
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1030
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 433
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 883
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 135
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 710
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 947
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5643
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 207
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7876
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1114
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5045
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33021
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 583
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3728
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3322
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.151260504201681e-4
allele num: 9520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25450
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.004894e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 3.304e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

QD
type: SiteQuality
SIO_000300: 1.171e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 882
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3352
bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 315
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 74
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1066
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 983
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1054
bin: 1.75e1
variant carriers: 4

GenotypeDepth
all individuals: 9143
bin: 1.25e1
variant carriers: 13

GenotypeDepth
all individuals: 518
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
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variant carriers: 1

GenotypeDepth
all individuals: 9036
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variant carriers: 0

GenotypeDepth
all individuals: 108
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variant carriers: 0

GenotypeDepth
all individuals: 27339
bin: 7.5e0
variant carriers: 5

GenotypeDepth
all individuals: 135
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1069
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 226
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1075
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5658
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 2

GenotypeQuality
all individuals: 4460
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9390
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variant carriers: 0

GenotypeQuality
all individuals: 30824
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1419
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 556
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 414
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 871
bin: 6.75e1
variant carriers: 2

Other
type: Population
allele count: 2
allele frequency: 4.926108374384237e-3
allele num: 406
num of homozygotes: 0

East Asian
type: Population
allele count: 22
allele frequency: 6.690997566909975e-3
allele num: 3288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23078
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2968
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.37439e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.85e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.099e0

FS
type: SiteQuality
SIO_000300: 3.234e0

QD
type: SiteQuality
SIO_000300: 1.121e1

MQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

GenotypeDepth
all individuals: 11320
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 25917
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 135
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9111
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 315
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 431
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1540
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2576
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variant carriers: 0

GenotypeDepth
all individuals: 1015
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variant carriers: 1

GenotypeDepth
all individuals: 226
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variant carriers: 0

GenotypeDepth
all individuals: 710
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variant carriers: 0

GenotypeDepth
all individuals: 945
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variant carriers: 0

GenotypeDepth
all individuals: 1048
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
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variant carriers: 0

GenotypeDepth
all individuals: 1066
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 882
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28399
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11775
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1993
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1460
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5642
bin: 9.75e1
variant carriers: 3