Disease: Coronary heart disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs7901695
TCF7L2
0.851 0.160 10 112994329 intron variant T/C snv 0.34 2
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs10923931
NOTCH2
0.925 0.120 1 119975336 intron variant G/T snv 0.17 2
rs17036101 0.925 0.120 3 12236345 regulatory region variant G/A;T snv 2
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 2
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 11
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs5215
KCNJ11
0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs6769511
IGF2BP2
0.925 0.120 3 185812502 intron variant T/C snv 0.46 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
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
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 3
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 4
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 3
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 3
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7