Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 4
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35