Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2254287
COL11A2
1.000 0.040 6 33176171 intron variant C/A;G;T snv 3
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 7
rs1501908 1.000 0.040 5 156971158 intergenic variant G/A;C;T snv 5
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 12
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 7
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 9
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs6544713
ABCG8
0.925 0.040 2 43846742 non coding transcript exon variant T/C snv 0.75 5
rs6756629
ABCG5 ; ABCG8
0.925 0.080 2 43837951 missense variant G/A;T snv 6.7E-02 5
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24