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rs7405696

From SNPedia

Orientationplus
Stabilizedplus
Make rs7405696(C;C)
Make rs7405696(C;G)
Make rs7405696(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position37742044
GeneHNF1B
is asnp
is mentioned by
dbSNPrs7405696
ebirs7405696
HLIrs7405696
Exacrs7405696
Varsomers7405696
Maprs7405696
PheGenIrs7405696
hapmaprs7405696
1000 genomesrs7405696
hgdprs7405696
ensemblrs7405696
gopubmedrs7405696
geneviewrs7405696
scholarrs7405696
googlers7405696
pharmgkbrs7405696
gwascentralrs7405696
openSNPrs7405696
23andMers7405696
23andMe allrs7405696
SNP Nexus

SNPshotrs7405696
SNPdbers7405696
MSV3drs7405696
GWAS Ctlgrs7405696
GMAF0.4059
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 21576123OA-icon.png] Large-scale fine mapping of the HNF1B locus and prostate cancer risk[PMID 18701471OA-icon.png] Chromosome 17q12 variants contribute to risk of early-onset prostate cancer.