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rs121908382

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908382(C;T)
Make rs121908382(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position45331530
GeneMUTYH
is asnp
is mentioned by
dbSNPrs121908382
ebirs121908382
HLIrs121908382
Exacrs121908382
Varsomers121908382
Maprs121908382
PheGenIrs121908382
hapmaprs121908382
1000 genomesrs121908382
hgdprs121908382
ensemblrs121908382
gopubmedrs121908382
geneviewrs121908382
scholarrs121908382
googlers121908382
pharmgkbrs121908382
gwascentralrs121908382
openSNPrs121908382
23andMers121908382
23andMe allrs121908382
SNP Nexus

SNPshotrs121908382
SNPdbers121908382
MSV3drs121908382
GWAS Ctlgrs121908382
Max Magnitude0
OMIM604933
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121908382(T;T)
Alt rs121908382(T;T)
Reference rs121908382(C;C)
Significance Pathogenic
Disease Neoplasm of stomach
Variation info
Gene MUTYH
CLNDBN Neoplasm of stomach
Reversed 1
HGVS NC_000001.10:g.45797202G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005619.5,