Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7501939
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.740 1.000 4 2008 2018
dbSNP: rs7501939
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma 		0.710 1.000 1 2011 2012
dbSNP: rs7501939
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41
CUI: C0201544
Disease: Prostate specific antigen measurement
Prostate specific antigen measurement 		0.700 1.000 1 2010 2010
dbSNP: rs7501939
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010