Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 7
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 8
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45 6
rs4905014
ITPK1
0.851 0.120 14 92945686 intron variant G/A;C snv 16
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs7115242
SIK3
0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7819412
XKR6
0.827 0.120 8 11187652 intron variant G/A;T snv 6
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 8
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5