SNP Links for Gene (Select 442867) - SNP

Select item 13254968111.

rs1325496811 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:24634468 (GRCh38)
Y:26780615 (GRCh37)
Canonical SPDI:: NC_000024.10:24634467:C:T
Gene:: BPY2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: T=0.079/70 (KOREAN)
HGVS:: NC_000024.10:g.24634468C>T, NC_000024.9:g.26780615C>T, NG_004755.2:g.2823582C>T

Select item 12927525732.

rs1292752573 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: Y:24634463 (GRCh38)
Y:26780610 (GRCh37)
Canonical SPDI:: NC_000024.10:24634462:C:G
Gene:: BPY2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: G=0.059/53 (KOREAN)
HGVS:: NC_000024.10:g.24634463C>G, NC_000024.9:g.26780610C>G, NG_004755.2:g.2823577C>G

Select item 12277012493.

rs1227701249 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: Y:24634731 (GRCh38)
Y:26780878 (GRCh37)
Canonical SPDI:: NC_000024.10:24634730:A:C,NC_000024.10:24634730:A:G
Gene:: BPY2B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: C=0.0003/1 (GnomAD)
G=0.088/107 (KOREAN)
HGVS:: NC_000024.10:g.24634731A>C, NC_000024.10:g.24634731A>G, NC_000024.9:g.26780878A>C, NC_000024.9:g.26780878A>G, NG_004755.2:g.2823845A>C, NG_004755.2:g.2823845A>G

Select item 3707100604.

rs370710060 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:24634806 (GRCh38)
Y:26780953 (GRCh37)
Canonical SPDI:: NC_000024.10:24634805:A:G
Gene:: BPY2B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.24634806A>G, NC_000024.9:g.26780953A>G, NG_004755.2:g.2823920A>G

Select item 1129969645.

rs112996964 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:24617782 (GRCh38)
Y:26763929 (GRCh37)
Canonical SPDI:: NC_000024.10:24617781:C:T
Gene:: BPY2B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.24617782C>T, NC_000024.9:g.26763929C>T, NG_004755.2:g.2806896C>T

Select item 1114415746.

rs111441574 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: Y:24630993 (GRCh38)
Y:26777140 (GRCh37)
Canonical SPDI:: NC_000024.10:24630992:A:G
Gene:: BPY2B (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000024.10:g.24630993A>G, NC_000024.9:g.26777140A>G, NG_004755.2:g.2820107A>G

Select item 1112379647.

rs111237964 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: Y:24617647 (GRCh38)
Y:26763794 (GRCh37)
Canonical SPDI:: NC_000024.10:24617646:C:T
Gene:: BPY2B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000024.10:g.24617647C>T, NC_000024.9:g.26763794C>T, NG_004755.2:g.2806761C>T

Select item 1637038.

rs163703 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: Y:24631011 (GRCh38)
Y:26777158 (GRCh37)
Canonical SPDI:: NC_000024.10:24631010:T:C
Gene:: BPY2B (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000024.10:g.24631011T>C, NC_000024.9:g.26777158T>C, NG_004755.2:g.2820125T>C

dbSNP