Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1722842 0.925 0.080 15 23785809 intron variant T/C snv 0.16 2
rs4804611
ZNF627
0.925 0.080 19 11617987 3 prime UTR variant A/G snv 0.24 2
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs1376251
TAS2R14 ; PRR4 ; PRH1 ; TAS2R50 ; PRH1-PRR4 ; PRH1-TAS2R14
0.882 0.160 12 10986253 missense variant C/T snv 0.40 0.28 3
rs17222842 0.882 0.120 13 30765980 downstream gene variant G/A snv 6.1E-02 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs2046934
MED12L ; P2RY12
0.882 0.200 3 151339854 intron variant G/A;C snv 3
rs2505083
JCAD
0.882 0.080 10 30046193 intron variant T/C snv 0.33 3
rs3744700
CXCL16
0.882 0.080 17 4734715 intron variant T/G snv 0.66 3
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
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
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37 4
rs150629733
AGTR1
0.851 0.080 3 148741190 missense variant T/C;G snv 4.0E-06; 8.8E-05 4
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 4
rs6131
SELP
0.851 0.200 1 169611647 missense variant C/T snv 0.20 0.22 4
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 4
rs7291467
LGALS2
0.851 0.160 22 37576621 intron variant G/A snv 0.49 4
rs8089
LOC101929523 ; THBS2
0.851 0.080 6 169217631 splice region variant A/C snv 0.22 4
rs9369640
PHACTR1
0.851 0.080 6 12901209 intron variant C/A;G snv 4
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs12526453
PHACTR1
0.827 0.160 6 12927312 intron variant C/G snv 0.27 5