Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11572325
CYP2J2
0.925 0.080 1 59896030 intron variant A/T snv 0.12 3
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs1177506410
AGT
0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 12
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs2890565
UTS2
0.732 0.440 1 7849677 missense variant C/T snv 8.7E-02 5.6E-02 15
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs5051
AGT
0.882 0.160 1 230714126 intron variant C/A;G;T snv 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1012841819
ADRA2B
0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 4
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs6742078
UGT1A3 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A6 ; UGT1A4 ; UGT1A9 ; UGT1A1 ; UGT1A5
0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs12487736
SCAP
1.000 0.080 3 47418189 missense variant C/T snv 0.54 0.47 2
rs12632110
SEMA3F
1.000 0.080 3 50186792 intron variant A/G snv 0.63 0.62 3
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52