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
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
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
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
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs17036101 0.925 0.120 3 12236345 regulatory region variant G/A;T snv 2
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 4
rs4607103
ADAMTS9-AS2
0.882 0.120 3 64726228 intron variant C/T snv 0.28 2
rs6769511
IGF2BP2
0.925 0.120 3 185812502 intron variant T/C snv 0.46 2
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs12518099
LINC01339
0.925 0.120 5 90250292 intron variant A/G;T snv 3
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 3
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
rs6931514
CDKAL1
0.925 0.120 6 20703721 intron variant A/G snv 0.27 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
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 3
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 4
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 4
rs2383208 0.882 0.120 9 22132077 downstream gene variant A/G;T snv 0.18 2
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7