Disease: Coronary heart disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10923931
NOTCH2
0.925 0.120 1 119975336 intron variant G/T snv 0.17 2
rs1153188 0.925 0.120 12 54705212 intergenic variant T/A snv 0.76 2
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 2
rs17036101 0.925 0.120 3 12236345 regulatory region variant G/A;T snv 2
rs2383208 0.882 0.120 9 22132077 downstream gene variant A/G;T snv 0.18 2
rs4607103
ADAMTS9-AS2
0.882 0.120 3 64726228 intron variant C/T snv 0.28 2
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs4712524
CDKAL1
0.925 0.120 6 20657634 intron variant A/G snv 0.40 2
rs5015480 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 2
rs6769511
IGF2BP2
0.925 0.120 3 185812502 intron variant T/C snv 0.46 2
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 2
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 3
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs5215
KCNJ11
0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 2
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 2
rs9300039 0.851 0.160 11 41893816 intergenic variant C/A snv 9.8E-02 3
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 2
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 3