Disease: Acute myocardial infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs770572030
LIPG
0.827 0.160 18 49581427 missense variant T/A;C snv 4.0E-06; 4.0E-06 5
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs771676129
CD36
0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs4244285
CYP2C19
0.695 0.360 10 94781859 synonymous variant G/A;C snv 0.18 18
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs7493
PON2
0.677 0.440 7 95405463 missense variant G/C snv 0.27 0.27 24