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: rs496892
rs496892
0.827 0.160 9 22024352 intron variant C/T snv 0.40
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2013 2013
dbSNP: rs496892
rs496892
0.827 0.160 9 22024352 intron variant C/T snv 0.40
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012
dbSNP: rs496892
rs496892
0.827 0.160 9 22024352 intron variant C/T snv 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2007 2007