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: rs1800961
rs1800961
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs1223493898
rs1223493898
0.851 0.120 20 44406090 missense variant G/A;C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
Cardiovascular Diseases 0.010 1.000 1 2012 2012