Gene: CAD ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs371150372
rs371150372
CAD
3 0.882 0.040 2 27223972 missense variant G/A;T snv 2.8E-05; 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs763172697
rs763172697
CAD
3 0.882 0.040 2 27233526 missense variant G/T snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs778916575
rs778916575
CAD
3 0.882 0.040 2 27222595 missense variant G/A snv 1.2E-05 0.010 1.000 1 2006 2006