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rs1016990

From SNPedia

Orientationminus
Stabilizedminus
Make rs1016990(C;C)
Make rs1016990(C;G)
Make rs1016990(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position37728924
GeneHNF1B
is asnp
is mentioned by
dbSNPrs1016990
ebirs1016990
HLIrs1016990
Exacrs1016990
Varsomers1016990
Maprs1016990
PheGenIrs1016990
hapmaprs1016990
1000 genomesrs1016990
hgdprs1016990
ensemblrs1016990
gopubmedrs1016990
geneviewrs1016990
scholarrs1016990
googlers1016990
pharmgkbrs1016990
gwascentralrs1016990
openSNPrs1016990
23andMers1016990
23andMe allrs1016990
SNP Nexus

SNPshotrs1016990
SNPdbers1016990
MSV3drs1016990
GWAS Ctlgrs1016990
GMAF0.2686
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 19168595OA-icon.png] Common variants of hepatocyte nuclear factor 1beta are associated with type 2 diabetes in a Chinese population.