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rs121913528

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913528(A;A)
Make rs121913528(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position25227349
GeneKRAS
is asnp
is mentioned by
dbSNPrs121913528
ebirs121913528
HLIrs121913528
Exacrs121913528
Varsomers121913528
Maprs121913528
PheGenIrs121913528
hapmaprs121913528
1000 genomesrs121913528
hgdprs121913528
ensemblrs121913528
gopubmedrs121913528
geneviewrs121913528
scholarrs121913528
googlers121913528
pharmgkbrs121913528
gwascentralrs121913528
openSNPrs121913528
23andMers121913528
23andMe allrs121913528
SNP Nexus

SNPshotrs121913528
SNPdbers121913528
MSV3drs121913528
GWAS Ctlgrs121913528
Max Magnitude0
OMIM190070
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121913528(A,T;A,T)
Alt rs121913528(A,T;A,T)
Reference rs121913528(G;G)
Significance Pathogenic
Disease not provided Bladder cancer
Variation info
Gene KRAS
CLNDBN not provided Bladder cancer, transitional cell, somatic
Reversed 1
HGVS NC_000012.11:g.25380283C>A; NC_000012.11:g.25380283C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000207502.1, RCV000013410.4,