Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
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
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 4
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
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1044250
ANGPTL4
0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29