Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1452231640 1.000 0.080 8 42339015 missense variant T/C snv 4.0E-06 4
rs1457547311 0.851 0.080 2 113131082 synonymous variant G/A snv 4.0E-06 4
rs4460629 0.882 0.080 1 155162859 intergenic variant T/C snv 0.56 4
rs4998557 0.851 0.080 21 31662579 intron variant G/A snv 0.22 4
rs6087990 0.925 0.080 20 32762102 upstream gene variant T/C;G snv 4
rs6458238
PGC
0.882 0.080 6 41749967 intron variant G/A;C snv 4
rs6733301 0.925 0.080 2 25053415 intron variant G/A snv 0.13 4
rs753724 0.882 0.080 10 94291660 intron variant G/A;C;T snv 4
rs8193 0.925 0.080 11 35229771 3 prime UTR variant C/T snv 0.29 4
rs881844 0.925 0.080 17 39653965 intron variant C/G snv 0.51 4
rs9589207 0.925 0.080 13 91351335 mature miRNA variant G/A;C snv 5.4E-03; 4.0E-06 4
rs9972882 0.925 0.080 17 39651445 intron variant A/C snv 0.66 4
rs1064261 0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06 3
rs111638916 0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3
rs1135354 0.925 0.080 2 102397842 3 prime UTR variant T/G snv 0.23 3
rs114673809 0.882 0.080 1 11787703 3 prime UTR variant G/A snv 5.0E-03 3
rs11564475 0.882 0.080 3 41238542 intron variant A/G snv 3.7E-02 3
rs115785973 0.925 0.080 17 78357871 3 prime UTR variant C/G;T snv 3
rs12083239 0.925 0.080 1 39985357 intergenic variant G/A;C snv 3
rs12155758 0.882 0.080 8 142684467 upstream gene variant G/A snv 0.23 3
rs12416605 0.925 0.080 10 29602331 mature miRNA variant C/T snv 0.22 0.20 3
rs12615966 0.882 0.080 2 104762499 upstream gene variant C/T snv 0.14 3
rs154268 0.925 0.080 5 40795766 intron variant C/T snv 0.69 3
rs158916 0.882 0.080 5 60949318 intron variant A/G snv 0.15 3
rs17033 0.925 0.080 4 99307788 3 prime UTR variant T/C snv 9.6E-02 3