Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1213545562
TH
1.000 0.080 11 2166984 synonymous variant G/A snv 9.6E-06 2
rs12487736
SCAP
1.000 0.080 3 47418189 missense variant C/T snv 0.54 0.47 2
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
rs16964543
ZNF536
1.000 0.080 19 30694303 intron variant T/C snv 0.32 2
rs4363
ACE
1.000 0.080 17 63497131 splice region variant G/A;C snv 0.52 2
rs7447815
SLC6A18
1.000 0.080 5 1240642 stop gained C/G;T snv 0.36; 7.6E-05 2
rs748702477
KCNMA1
1.000 0.080 10 77110278 synonymous variant A/G snv 1.4E-05 2
rs11572325
CYP2J2
0.925 0.080 1 59896030 intron variant A/T snv 0.12 3
rs12632110
SEMA3F
1.000 0.080 3 50186792 intron variant A/G snv 0.63 0.62 3
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
rs197922
GOSR2 ; LRRC37A2
0.925 0.080 17 46931204 missense variant G/A snv 0.35 0.33 3
rs2301339
CDCA3 ; GNB3
1.000 0.080 12 6845460 3 prime UTR variant G/A;T snv 3
rs5629
PTGIS
0.925 0.080 20 49513169 stop gained G/A;T snv 4.0E-06; 0.25 3
rs755703581
PDX1
0.925 0.120 13 27920295 missense variant G/A snv 2.3E-05 7.0E-06 3
rs7913948
ALOX5
1.000 0.080 10 45373441 upstream gene variant G/A snv 0.17 3
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
rs1334899057
SSTR4
0.882 0.160 20 23035908 missense variant T/C snv 7.0E-06 4
rs1462059537
EDNRA
0.882 0.160 4 147535944 missense variant C/T snv 8.0E-06 4
rs1801058
GRK4
0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 4
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4
rs758801521
ADRA1A
0.882 0.160 8 26770618 missense variant A/G snv 4.0E-06 4
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5