Have questions? Visit https://www.reddit.com/r/SNPedia

rs3760511

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) normal risk for prostate cancer
(A;C) 1.16x increased risk for prostate cancer
(C;C) 1.16x increased risk for prostate cancer
(G;G) 1.2
ReferenceGRCh38 38.1/141
Chromosome17
Position37746322
GeneHNF1B
is asnp
is mentioned by
dbSNPrs3760511
ebirs3760511
HLIrs3760511
Exacrs3760511
Varsomers3760511
Maprs3760511
PheGenIrs3760511
hapmaprs3760511
1000 genomesrs3760511
hgdprs3760511
ensemblrs3760511
gopubmedrs3760511
geneviewrs3760511
scholarrs3760511
googlers3760511
pharmgkbrs3760511
gwascentralrs3760511
openSNPrs3760511
23andMers3760511
23andMe allrs3760511
SNP Nexus

SNPshotrs3760511
SNPdbers3760511
MSV3drs3760511
GWAS Ctlgrs3760511
GMAF0.3751
Max Magnitude1.2
? (A;A) (A;C) (C;C) 28
rs3760511 increases susceptibility to Prostate cancer 1.16 times for carriers of the C allele [PMID 17603485]


[PMID 19168595OA-icon.png] Common variants of hepatocyte nuclear factor 1beta are associated with type 2 diabetes in a Chinese population.


[PMID 20690139] Meta-analysis of genome-wide and replication association studies on prostate cancer.


[PMID 24422606] Assessment of Association between Common Variants at 17q12 and Prostate Cancer Risk-Evidence from Serbian Population and Meta-Analysis