Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs11668477 0.925 0.080 19 11084354 downstream gene variant A/G snv 0.34 7
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 8
rs440446
APOE
0.807 0.200 19 44905910 missense variant C/G;T snv 0.60 8
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs1864163
CETP
0.882 0.120 16 56963321 intron variant G/A snv 0.26 10
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs5880
CETP
0.827 0.040 16 56981179 missense variant G/C snv 5.2E-02 3.7E-02 10