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: rs7049105
rs7049105
0.807 0.120 9 22028802 intron variant A/G snv 0.58
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 1 2007 2007
dbSNP: rs7049105
rs7049105
0.807 0.120 9 22028802 intron variant A/G snv 0.58
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2013 2013
dbSNP: rs7049105
rs7049105
0.807 0.120 9 22028802 intron variant A/G snv 0.58
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.700 1.000 1 2011 2011
dbSNP: rs7049105
rs7049105
0.807 0.120 9 22028802 intron variant A/G snv 0.58
CUI: C0017638
Disease: Glioma
Glioma
0.700 1.000 1 2011 2011
dbSNP: rs7049105
rs7049105
0.807 0.120 9 22028802 intron variant A/G snv 0.58
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012