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: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.830 1.000 3 2008 2013
dbSNP: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		0.700 1.000 1 2012 2012
dbSNP: rs17483466
rs17483466
ACOXL ; MIR4435-2HG
0.827 0.280 2 111039881 intron variant A/G snv 0.15
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010