Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs1310478538
C3
0.851 0.080 19 6713295 missense variant C/G snv 1.4E-05 4
rs1333046
CDKN2B-AS1
0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs150629733
AGTR1
0.851 0.080 3 148741190 missense variant T/C;G snv 4.0E-06; 8.8E-05 4
rs1722842 0.925 0.080 15 23785809 intron variant T/C snv 0.16 2
rs1866389
THBS4
0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 9
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs2505083
JCAD
0.882 0.080 10 30046193 intron variant T/C snv 0.33 3
rs264
LPL
0.882 0.080 8 19955669 intron variant G/A snv 0.14 6
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 4
rs3744700
CXCL16
0.882 0.080 17 4734715 intron variant T/G snv 0.66 3
rs3785889
GOSR2 ; LRRC37A2
0.827 0.080 17 46928464 intron variant G/A snv 0.45 5
rs4804611
ZNF627
0.925 0.080 19 11617987 3 prime UTR variant A/G snv 0.24 2
rs6046
F7
0.925 0.080 13 113118845 missense variant G/A;C;T snv 0.13 5
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 4
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 6
rs7213516 0.882 0.080 17 63474189 upstream gene variant G/A snv 5.7E-02 3
rs749903604
APOB
0.882 0.080 2 21042450 missense variant G/A snv 8.0E-06 3
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs756351287
PLA2G1B
0.827 0.080 12 120325936 missense variant G/A;C;T snv 2.4E-05 5
rs771676129
CD36
0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs8089
LOC101929523 ; THBS2
0.851 0.080 6 169217631 splice region variant A/C snv 0.22 4