Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012841819
ADRA2B
0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 4
rs1024323
GRK4
0.882 0.160 4 3004316 missense variant C/A;G;T snv 0.36 4
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1213545562
TH
1.000 0.080 11 2166984 synonymous variant G/A snv 9.6E-06 2
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs1380959039
KCNMA1
1.000 0.080 10 77086524 synonymous variant A/G snv 4.0E-06 2
rs1384915680
TH
1.000 0.080 11 2166903 synonymous variant G/A snv 4.3E-06 2
rs1462059537
EDNRA
0.882 0.160 4 147535944 missense variant C/T snv 8.0E-06 4
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs17222772
ALOX5AP
0.925 0.120 13 30737959 intron variant A/T snv 3
rs17231896
CETP
0.925 0.120 16 56982180 missense variant G/A;C snv 3
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1801058
GRK4
0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 4
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121