Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12522248
HAVCR1
0.925 0.080 5 157052415 missense variant T/C snv 0.29 0.26 2
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs231150
TRPS1
0.925 0.080 8 115408099 downstream gene variant A/T snv 0.55 2
rs3093100
CYP4F2
0.925 0.080 19 15897659 5 prime UTR variant C/G;T snv 0.15; 5.9E-05 2
rs3093105
CYP4F2
0.925 0.080 19 15897578 missense variant A/C snv 0.16 0.18 2
rs3093135
CYP4F2
0.925 0.080 19 15893561 intron variant A/T snv 0.15 3
rs3759387
MVK ; MMAB
0.925 0.080 12 109574662 intron variant G/T snv 0.31 2
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 6
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs9860747 0.925 0.080 3 186869628 regulatory region variant T/C snv 0.70 2
rs10937273 0.882 0.160 3 186831906 downstream gene variant G/A snv 0.33 4
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs2740483
ABCA1 ; LOC105376196
0.882 0.120 9 104928254 intron variant G/C snv 0.75 3
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs7395662 0.882 0.080 11 48497341 downstream gene variant A/G snv 0.56 5
rs12495941
ADIPOQ
0.851 0.280 3 186850391 intron variant G/T snv 0.35 5
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs17366568
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 6
rs2287218
MVK
0.851 0.080 12 109581533 synonymous variant C/T snv 0.16 0.17 4
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs6131
SELP
0.851 0.200 1 169611647 missense variant C/T snv 0.20 0.22 4
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs10118757
MTAP
0.827 0.120 9 21853340 intron variant A/G snv 0.26 7