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: rs735665
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		0.840 1.000 4 2008 2018
dbSNP: rs735665
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15
CUI: C0242350
Disease: Erectile dysfunction
Erectile dysfunction 		0.700 1.000 1 2012 2012
dbSNP: rs735665
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular 		0.700 1.000 1 2010 2010
dbSNP: rs735665
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15
CUI: C2931822
Disease: Nasopharyngeal carcinoma
Nasopharyngeal carcinoma 		0.700 1.000 1 2010 2010