Disease: Coronary Artery Disease
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs61776719 0.776 0.120 1 37995647 downstream gene variant C/A snv 0.46 11
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 9
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 9
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 5
rs606452
SERPINH1
1.000 0.040 11 75565133 intron variant A/C snv 0.78 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
rs2814993
ILRUN
1.000 0.040 6 34651116 intron variant G/A snv 0.17 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