rs3764613 - SNP

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Select item 37646131.

rs3764613 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:46392960 (GRCh38)
19:46896217 (GRCh37)
Canonical SPDI:: NC_000019.10:46392959:A:G
Gene:: LOC105372426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.444657/68013 (ALFA)
G=0.220478/646 (KOREAN)
G=0.22381/47 (Vietnamese)
A=0.25/6 (PRJEB36033)
A=0.3/12 (GENOME_DK)
G=0.345955/5798 (TOMMO)
A=0.371257/124 (SGDP_PRJ)
A=0.407888/1572 (ALSPAC)
G=0.410525/2056 (1000Genomes)
G=0.42161/796 (HapMap)
A=0.424218/1573 (TWINSUK)
A=0.432866/432 (GoNL)
A=0.470588/16 (Siberian)
A=0.476852/103 (Qatari)
A=0.489955/2195 (Estonian)
G=0.491667/295 (NorthernSweden)
G=0.495323/131107 (TOPMED)
A=0.499314/69909 (GnomAD)
HGVS:: NC_000019.10:g.46392960A>G, NC_000019.9:g.46896217A>G, NG_028163.1:g.50967A>G, XR_936001.3:n.1078T>C, XR_936001.2:n.2194T>C, XR_936001.1:n.2178T>C

Select item 176606012.

rs17660601 has merged into rs3764613 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:46392960 (GRCh38)
19:46896217 (GRCh37)
Canonical SPDI:: NC_000019.10:46392959:A:G
Gene:: LOC105372426 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.444657/68013 (ALFA)
G=0.220478/646 (KOREAN)
G=0.22381/47 (Vietnamese)
A=0.25/6 (PRJEB36033)
A=0.3/12 (GENOME_DK)
G=0.345955/5798 (TOMMO)
A=0.371257/124 (SGDP_PRJ)
A=0.407888/1572 (ALSPAC)
G=0.410525/2056 (1000Genomes)
G=0.42161/796 (HapMap)
A=0.424218/1573 (TWINSUK)
A=0.432866/432 (GoNL)
A=0.470588/16 (Siberian)
A=0.476852/103 (Qatari)
A=0.489955/2195 (Estonian)
G=0.491667/295 (NorthernSweden)
G=0.495323/131107 (TOPMED)
A=0.499314/69909 (GnomAD)
HGVS:: NC_000019.10:g.46392960A>G, NC_000019.9:g.46896217A>G, NG_028163.1:g.50967A>G, XR_936001.3:n.1078T>C, XR_936001.2:n.2194T>C, XR_936001.1:n.2178T>C