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: rs1169288
rs1169288
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.730 1.000 2 2009 2018
dbSNP: rs2244608
rs2244608
0.882 0.160 12 120979185 intron variant A/G snv 0.29
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.700 1.000 3 2017 2018