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rs121908381

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908381(G;T)
Make rs121908381(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position45331220
GeneMUTYH
is asnp
is mentioned by
dbSNPrs121908381
ebirs121908381
HLIrs121908381
Exacrs121908381
Varsomers121908381
Maprs121908381
PheGenIrs121908381
hapmaprs121908381
1000 genomesrs121908381
hgdprs121908381
ensemblrs121908381
gopubmedrs121908381
geneviewrs121908381
scholarrs121908381
googlers121908381
pharmgkbrs121908381
gwascentralrs121908381
openSNPrs121908381
23andMers121908381
23andMe allrs121908381
SNP Nexus

SNPshotrs121908381
SNPdbers121908381
MSV3drs121908381
GWAS Ctlgrs121908381
Max Magnitude0
OMIM604933
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908381(T;T)
Alt rs121908381(T;T)
Reference rs121908381(G;G)
Significance Pathogenic
Disease MYH-associated polyposis Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene MUTYH
CLNDBN MYH-associated polyposis Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 1
HGVS NC_000001.10:g.45796892C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000005618.4, RCV000222872.1, RCV000235388.1,