Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7
rs2306235
PLEKHO1
0.827 0.040 1 150150942 missense variant C/G;T snv 1.1E-02; 1.6E-05 4.4E-03 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs2516839
USF1
0.732 0.320 1 161043331 5 prime UTR variant C/T snv 0.49 14
rs3045215
IRF2BP2
0.882 0.040 1 234605171 3 prime UTR variant -/GTTACAATA;GTTATAATA delins 3
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs313152
PTAFR
0.851 0.120 1 28149490 3 prime UTR variant T/C snv 0.29 4
rs35511654
TMIGD3 ; ADORA3
0.882 0.040 1 111500165 missense variant T/G snv 9.4E-02 9.8E-02 3
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs3931020 0.882 0.040 1 74769633 downstream gene variant T/C snv 0.71 4
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4537545
IL6R
0.790 0.160 1 154446403 intron variant C/T snv 0.48 11
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs5063
CLCN6 ; NPPA-AS1 ; NPPA
0.763 0.280 1 11847591 missense variant C/T snv 5.6E-02 5.3E-02 12
rs5065
NPPA ; CLCN6 ; NPPA-AS1
0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs5705
REN
0.882 0.040 1 204162058 synonymous variant T/G snv 0.14 0.18 3
rs5938
PTAFR
0.827 0.200 1 28150351 missense variant G/T snv 8.0E-03 2.5E-03 5
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs6020
F5
0.882 0.040 1 169549874 missense variant C/T snv 0.11 0.12 3
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9