Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs2254298 0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs3135932 0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2023239 0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs80356616 0.732 0.360 11 17387917 missense variant C/T snv 19
rs324981 0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs6354 0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs821616 0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs9470080 0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs10994336 0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs2710102 0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10