Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs3918226
NOS3
0.925 0.080 7 150993088 intron variant C/T snv 5.7E-02 12
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs11014166
CACNB2
0.882 0.040 10 18419869 intron variant A/T snv 0.27 10
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681492
ATP2B1
0.925 0.040 12 89619312 intron variant T/C;G snv 10
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs16948048
ZNF652 ; LOC102724596
0.925 0.040 17 49363104 intron variant A/G snv 0.37 8
rs17608766
LRRC37A2 ; GOSR2
1.000 0.040 17 46935905 3 prime UTR variant T/C snv 9.2E-02 8
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5