Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10755578
LPA
0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42 2
rs11057401
CCDC92
0.925 0.040 12 123942759 missense variant T/A snv 0.27 0.30 2
rs11881940
HNRNPUL1 ; TGFB1
0.925 0.040 19 41302527 non coding transcript exon variant A/C;G;T snv 4.9E-06; 4.9E-06; 0.14 2
rs1541861
NOS3
0.925 0.040 7 151000245 intron variant C/A snv 0.70 2
rs16874954
PLA2G7
0.925 0.040 6 46709361 missense variant C/A snv 2
rs17114046
PLPP3
0.925 0.040 1 56500678 intron variant A/G snv 0.12 2
rs2133189
MIA3
0.925 0.040 1 222641100 intron variant C/T snv 0.56 2
rs216172
SMG6
0.925 0.040 17 2223210 intron variant G/C snv 0.35 2
rs2246942
LIPA
0.925 0.040 10 89245129 intron variant A/C;G snv 2
rs2306374
MRAS
0.925 0.040 3 138401110 intron variant T/C snv 0.12 2
rs3127599
LPAL2
0.925 0.040 6 160486102 intron variant C/T snv 0.28 2
rs3746731
CD93
0.925 0.040 20 23084572 missense variant G/A snv 0.57 0.50 2
rs4290 0.925 0.040 17 63474767 upstream gene variant C/A;T snv 2
rs7767084
LPA
0.925 0.040 6 160541471 intron variant T/C snv 0.13 2
rs840616
LOC105373786
0.925 0.040 2 187331742 intron variant T/C snv 0.56 2
rs9508025
FLT1
0.925 0.040 13 28409926 intron variant C/G;T snv 2
rs10159239
NLRP3
0.882 0.040 1 247443750 intron variant G/A snv 0.57 3
rs1051339
LIPA
0.882 0.040 10 89247582 missense variant C/T snv 9.5E-02 0.13 3
rs10918859
NOS1AP
0.882 0.040 1 162199478 intron variant G/A snv 0.16 3
rs12040273
GALNT2
0.882 0.040 1 230063651 intron variant C/T snv 0.28 3
rs12115090
CRISPLD1
0.882 0.040 8 75012585 intron variant A/C snv 0.33 0.44 3
rs12344245
FAM189A2
0.882 0.040 9 69340801 intron variant A/G snv 0.12 3
rs12704673
CALCR
0.882 0.040 7 93525009 intron variant A/G;T snv 0.27 3
rs1351855165
DUOX2
0.882 0.040 15 45111550 synonymous variant G/A snv 3
rs138760780
CDK18
0.882 0.040 1 205515245 intron variant C/T snv 1.5E-02 3