Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1801282
rs1801282
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.060 1.000 6 2005 2012
dbSNP: rs1805192
rs1805192
0.510 0.840 3 12379739 missense variant C/G snv
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.060 1.000 6 2005 2012
dbSNP: rs3856806
rs3856806
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
Cardiovascular Diseases 0.030 1.000 3 2012 2016