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: rs7176508
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.830 1.000 4 2008 2014
dbSNP: rs7176508
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010
dbSNP: rs7176508
rs7176508
DRAIC
0.851 0.280 15 69726651 intron variant A/G snv 0.67
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		0.700 1.000 1 2012 2012