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rs4971052

From SNPedia

Orientationplus
Stabilizedplus
Make rs4971052(C;C)
Make rs4971052(C;T)
Make rs4971052(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position155153542
is asnp
is mentioned by
dbSNPrs4971052
ebirs4971052
HLIrs4971052
Exacrs4971052
Varsomers4971052
Maprs4971052
PheGenIrs4971052
hapmaprs4971052
1000 genomesrs4971052
hgdprs4971052
ensemblrs4971052
gopubmedrs4971052
geneviewrs4971052
scholarrs4971052
googlers4971052
pharmgkbrs4971052
gwascentralrs4971052
openSNPrs4971052
23andMers4971052
23andMe allrs4971052
SNP Nexus

SNPshotrs4971052
SNPdbers4971052
MSV3drs4971052
GWAS Ctlgrs4971052
GMAF0.4702
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19924550OA-icon.png] A comprehensive analysis of common genetic variation in MUC1, MUC5AC, MUC6 genes and risk of stomach cancer