Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs3774261
ADIPOQ ; ADIPOQ-AS1
0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3834458
FADS1 ; FADS2
0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs3772622
AGTR1
0.851 0.080 3 148717966 intron variant T/A;C snv 4
rs16996148 0.882 0.120 19 19547663 downstream gene variant G/T snv 0.10 8
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs1263173 0.925 0.080 11 116810292 downstream gene variant G/A snv 0.53 4