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rs4276913

From SNPedia

Orientationplus
Stabilizedplus
Make rs4276913(A;A)
Make rs4276913(A;G)
Make rs4276913(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position155159197
is asnp
is mentioned by
dbSNPrs4276913
dbSNP (classic)rs4276913
ClinGenrs4276913
ebirs4276913
HLIrs4276913
Exacrs4276913
Gnomadrs4276913
Varsomers4276913
LitVarrs4276913
Maprs4276913
PheGenIrs4276913
Biobankrs4276913
1000 genomesrs4276913
hgdprs4276913
ensemblrs4276913
geneviewrs4276913
scholarrs4276913
googlers4276913
pharmgkbrs4276913
gwascentralrs4276913
openSNPrs4276913
23andMers4276913
SNPshotrs4276913
SNPdbers4276913
MSV3drs4276913
GWAS Ctlgrs4276913
GMAF0.4986
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 19924550OA-icon.png] A comprehensive analysis of common genetic variation in MUC1, MUC5AC, MUC6 genes and risk of stomach cancer