rs2432661 - SNP

Select item 24326611.

rs2432661 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:38125497 (GRCh38)
2:38352639 (GRCh37)
Canonical SPDI:: NC_000002.12:38125496:T:C
Gene:: LOC107985871 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.364022/73598 (ALFA)
C=0.084112/18 (Vietnamese)
C=0.100184/1679 (TOMMO)
C=0.118089/346 (KOREAN)
C=0.126092/231 (Korea1K)
C=0.256238/534 (HGDP_Stanford)
C=0.258475/488 (HapMap)
C=0.268114/1343 (1000Genomes)
C=0.310665/82230 (TOPMED)
C=0.318943/44654 (GnomAD)
C=0.335938/1505 (Estonian)
C=0.351402/1303 (TWINSUK)
C=0.363333/218 (NorthernSweden)
C=0.369486/1424 (ALSPAC)
C=0.375/15 (GENOME_DK)
C=0.37963/82 (Qatari)
C=0.390782/390 (GoNL)
T=0.410256/96 (SGDP_PRJ)
T=0.45/18 (PRJEB36033)
T=0.454545/10 (Siberian)
HGVS:: NC_000002.12:g.38125497T>C, NC_000002.11:g.38352639T>C

Select item 576077042.

rs57607704 has merged into rs2432661 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:38125497 (GRCh38)
2:38352639 (GRCh37)
Canonical SPDI:: NC_000002.12:38125496:T:C
Gene:: LOC107985871 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.364022/73598 (ALFA)
C=0.084112/18 (Vietnamese)
C=0.100184/1679 (TOMMO)
C=0.118089/346 (KOREAN)
C=0.126092/231 (Korea1K)
C=0.256238/534 (HGDP_Stanford)
C=0.258475/488 (HapMap)
C=0.268114/1343 (1000Genomes)
C=0.310665/82230 (TOPMED)
C=0.318943/44654 (GnomAD)
C=0.335938/1505 (Estonian)
C=0.351402/1303 (TWINSUK)
C=0.363333/218 (NorthernSweden)
C=0.369486/1424 (ALSPAC)
C=0.375/15 (GENOME_DK)
C=0.37963/82 (Qatari)
C=0.390782/390 (GoNL)
T=0.410256/96 (SGDP_PRJ)
T=0.45/18 (PRJEB36033)
T=0.454545/10 (Siberian)
HGVS:: NC_000002.12:g.38125497T>C, NC_000002.11:g.38352639T>C

Select item 174128803.

rs17412880 has merged into rs2432661 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:38125497 (GRCh38)
2:38352639 (GRCh37)
Canonical SPDI:: NC_000002.12:38125496:T:C
Gene:: LOC107985871 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.364022/73598 (ALFA)
C=0.084112/18 (Vietnamese)
C=0.100184/1679 (TOMMO)
C=0.118089/346 (KOREAN)
C=0.126092/231 (Korea1K)
C=0.256238/534 (HGDP_Stanford)
C=0.258475/488 (HapMap)
C=0.268114/1343 (1000Genomes)
C=0.310665/82230 (TOPMED)
C=0.318943/44654 (GnomAD)
C=0.335938/1505 (Estonian)
C=0.351402/1303 (TWINSUK)
C=0.363333/218 (NorthernSweden)
C=0.369486/1424 (ALSPAC)
C=0.375/15 (GENOME_DK)
C=0.37963/82 (Qatari)
C=0.390782/390 (GoNL)
T=0.410256/96 (SGDP_PRJ)
T=0.45/18 (PRJEB36033)
T=0.454545/10 (Siberian)
HGVS:: NC_000002.12:g.38125497T>C, NC_000002.11:g.38352639T>C

dbSNP