Disease: Coronary Arteriosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs1049255
CYBA
0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 9
rs2576178
RNLS ; LIPJ
0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5