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rs13156930

From SNPedia

Orientationplus
Stabilizedplus
Make rs13156930(C;C)
Make rs13156930(C;G)
Make rs13156930(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position44697933
is asnp
is mentioned by
dbSNPrs13156930
ebirs13156930
HLIrs13156930
Exacrs13156930
Varsomers13156930
Maprs13156930
PheGenIrs13156930
hapmaprs13156930
1000 genomesrs13156930
hgdprs13156930
ensemblrs13156930
gopubmedrs13156930
geneviewrs13156930
scholarrs13156930
googlers13156930
pharmgkbrs13156930
gwascentralrs13156930
openSNPrs13156930
23andMers13156930
23andMe allrs13156930
SNP Nexus

SNPshotrs13156930
SNPdbers13156930
MSV3drs13156930
GWAS Ctlgrs13156930
GMAF0.489
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 20140701OA-icon.png] Genetic variants on chromosome 5p12 are associated with risk of breast cancer in African American women: the Black Women's Health Study