rs232620 - SNP

Select item 2326201.

rs232620 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:38131522 (GRCh38)
2:38358664 (GRCh37)
Canonical SPDI:: NC_000002.12:38131521:A:G
Gene:: CYP1B1-AS1 (Varview), LOC107985871 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.33701/52943 (ALFA)
G=0.028302/6 (Vietnamese)
G=0.049579/831 (TOMMO)
G=0.061602/180 (KOREAN)
G=0.072052/132 (Korea1K)
G=0.226577/1135 (1000Genomes)
G=0.228571/432 (HapMap)
G=0.280539/74256 (TOPMED)
G=0.286718/40168 (GnomAD)
G=0.297125/186 (Chileans)
G=0.3/12 (GENOME_DK)
G=0.3/339 (Daghestan)
G=0.313333/188 (NorthernSweden)
G=0.323894/1201 (TWINSUK)
G=0.333705/1495 (Estonian)
G=0.339128/1307 (ALSPAC)
G=0.360721/360 (GoNL)
G=0.393519/85 (Qatari)
A=0.401869/86 (SGDP_PRJ)
A=0.5/12 (Siberian)
HGVS:: NC_000002.12:g.38131522A>G, NC_000002.11:g.38358664A>G, NR_027252.1:n.98A>G, NM_173652.1:c.-351A>G

Select item 3865650032.

rs386565003 has merged into rs232620 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:38131522 (GRCh38)
2:38358664 (GRCh37)
Canonical SPDI:: NC_000002.12:38131521:A:G
Gene:: CYP1B1-AS1 (Varview), LOC107985871 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.33701/52943 (ALFA)
G=0.028302/6 (Vietnamese)
G=0.049579/831 (TOMMO)
G=0.061602/180 (KOREAN)
G=0.072052/132 (Korea1K)
G=0.226577/1135 (1000Genomes)
G=0.228571/432 (HapMap)
G=0.280539/74256 (TOPMED)
G=0.286718/40168 (GnomAD)
G=0.297125/186 (Chileans)
G=0.3/12 (GENOME_DK)
G=0.3/339 (Daghestan)
G=0.313333/188 (NorthernSweden)
G=0.323894/1201 (TWINSUK)
G=0.333705/1495 (Estonian)
G=0.339128/1307 (ALSPAC)
G=0.360721/360 (GoNL)
G=0.393519/85 (Qatari)
A=0.401869/86 (SGDP_PRJ)
A=0.5/12 (Siberian)
HGVS:: NC_000002.12:g.38131522A>G, NC_000002.11:g.38358664A>G, NR_027252.1:n.98A>G, NM_173652.1:c.-351A>G

Select item 174129153.

rs17412915 has merged into rs232620 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:38131522 (GRCh38)
2:38358664 (GRCh37)
Canonical SPDI:: NC_000002.12:38131521:A:G
Gene:: CYP1B1-AS1 (Varview), LOC107985871 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.33701/52943 (ALFA)
G=0.028302/6 (Vietnamese)
G=0.049579/831 (TOMMO)
G=0.061602/180 (KOREAN)
G=0.072052/132 (Korea1K)
G=0.226577/1135 (1000Genomes)
G=0.228571/432 (HapMap)
G=0.280539/74256 (TOPMED)
G=0.286718/40168 (GnomAD)
G=0.297125/186 (Chileans)
G=0.3/12 (GENOME_DK)
G=0.3/339 (Daghestan)
G=0.313333/188 (NorthernSweden)
G=0.323894/1201 (TWINSUK)
G=0.333705/1495 (Estonian)
G=0.339128/1307 (ALSPAC)
G=0.360721/360 (GoNL)
G=0.393519/85 (Qatari)
A=0.401869/86 (SGDP_PRJ)
A=0.5/12 (Siberian)
HGVS:: NC_000002.12:g.38131522A>G, NC_000002.11:g.38358664A>G, NR_027252.1:n.98A>G, NM_173652.1:c.-351A>G

dbSNP