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Select item 76411281.

rs7641128 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 3:36800266 (GRCh38)
3:36841757 (GRCh37)
Canonical SPDI:: NC_000003.12:36800265:G:A,NC_000003.12:36800265:G:C,NC_000003.12:36800265:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.251634/4467 (ALFA)
C=0.093458/20 (Vietnamese)
C=0.140284/257 (Korea1K)
C=0.141277/1022 (Korea4K)
C=0.153662/449 (KOREAN)
G=0.222991/999 (Estonian)
G=0.238333/143 (NorthernSweden)
G=0.241483/241 (GoNL)
G=0.267677/106 (SGDP_PRJ)
G=0.269447/40167 (GnomAD_genomes)
G=0.270496/1003 (TWINSUK)
G=0.275298/1061 (ALSPAC)
G=0.280313/74196 (TOPMED)
G=0.287037/62 (Qatari)
G=0.382417/2449 (1000Genomes_30X)
G=0.390775/1957 (1000Genomes)
G=0.5/3 (Siberian)
HGVS:: NC_000003.12:g.36800266G>A, NC_000003.12:g.36800266G>C, NC_000003.12:g.36800266G>T, NC_000003.11:g.36841757G>A, NC_000003.11:g.36841757G>C, NC_000003.11:g.36841757G>T

Supplemental Content

dbSNP