Disease: Coronary heart disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 4
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 2
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs7578597
THADA
0.807 0.240 2 43505684 missense variant T/C snv 9.9E-02 0.14 2
rs7754840
CDKAL1
0.807 0.200 6 20661019 intron variant G/A;C;T snv 3
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
rs5215
KCNJ11
0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 2
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 4