Disease: Acute myocardial infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs281865545
PECAM1
0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
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
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs699947
VEGFA
0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67