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: rs944797
rs944797
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.800 1.000 3 2011 2013
dbSNP: rs944797
rs944797
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 2 2011 2013
dbSNP: rs944797
rs944797
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49
Ankle brachial pressure index (observable entity)
0.700 1.000 1 2012 2012
dbSNP: rs944797
rs944797
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49
CUI: C0017638
Disease: Glioma
Glioma
0.700 1.000 1 2011 2011
dbSNP: rs944797
rs944797
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012