Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs2066808
STAT2
0.807 0.280 12 56344189 intron variant A/G snv 0.21 8
rs6234
PCSK1 ; LOC101929710
0.851 0.160 5 96393270 missense variant G/C snv 0.27 0.24 8
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 4
rs2814993
ILRUN
1.000 0.040 6 34651116 intron variant G/A snv 0.17 3
rs7087507
ARID5B
0.925 0.120 10 61985930 intron variant A/G snv 0.33 3
rs10818576
DAB2IP
1.000 0.040 9 121650669 intron variant T/G snv 0.21 2
rs13734
RRBP1
1.000 0.040 20 17614084 3 prime UTR variant G/A snv 0.15 2
rs57265257
NOA1
1.000 0.040 4 56973114 intron variant A/T snv 0.22 0.20 2
rs659418
SERPINH1
1.000 0.040 11 75573289 downstream gene variant T/G snv 0.19 2