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rs6761391

From SNPedia

Orientationplus
Stabilizedplus
Make rs6761391(C;C)
Make rs6761391(C;G)
Make rs6761391(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position127396708
is asnp
is mentioned by
dbSNPrs6761391
ebirs6761391
HLIrs6761391
Exacrs6761391
Varsomers6761391
Maprs6761391
PheGenIrs6761391
hapmaprs6761391
1000 genomesrs6761391
hgdprs6761391
ensemblrs6761391
gopubmedrs6761391
geneviewrs6761391
scholarrs6761391
googlers6761391
pharmgkbrs6761391
gwascentralrs6761391
openSNPrs6761391
23andMers6761391
23andMe allrs6761391
SNP Nexus

SNPshotrs6761391
SNPdbers6761391
MSV3drs6761391
GWAS Ctlgrs6761391
GMAF0.3981
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 21455670] Genetic variation in genes encoding for polymerase ? subunits associates with breast cancer risk, tumour characteristics and survival