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: rs10120688
rs10120688
0.807 0.080 9 22056500 intron variant G/A snv 0.50
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.710 1.000 1 2012 2012
dbSNP: rs10120688
rs10120688
0.807 0.080 9 22056500 intron variant G/A snv 0.50
CUI: C0017638
Disease: Glioma
Glioma
0.700 1.000 1 2011 2011
dbSNP: rs10120688
rs10120688
0.807 0.080 9 22056500 intron variant G/A snv 0.50
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery
0.700 1.000 1 2013 2013
dbSNP: rs10120688
rs10120688
0.807 0.080 9 22056500 intron variant G/A snv 0.50
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012