Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs652438 0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs3740393 0.776 0.280 10 102876898 intron variant G/C;T snv 10
rs1192694481 0.882 0.080 11 102955629 missense variant C/T snv 4.0E-06 4
rs745564626 0.752 0.280 14 103699003 missense variant C/G;T snv 4.3E-05 14
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1297812518 0.763 0.160 14 103707168 missense variant G/A snv 1.3E-05 1.4E-05 9
rs9295535 0.851 0.160 6 10439735 mature miRNA variant T/C snv 0.30 0.20 4
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs507879 0.882 0.080 11 105007200 missense variant T/A;C;G snv 0.43 0.49 3
rs1467453450 0.882 0.080 9 105506513 missense variant A/G snv 7.0E-06 4
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs419558 0.882 0.080 4 106922935 3 prime UTR variant C/T snv 0.29 3
rs17037102 0.807 0.240 4 106924637 missense variant C/A;T snv 0.15 6
rs17723637 0.882 0.080 9 106925122 missense variant A/G snv 0.14 0.13 3
rs447372 0.882 0.080 4 106932839 intron variant G/A snv 0.48 3
rs4262299 0.882 0.080 8 107330035 intron variant A/C;T snv 3
rs1654701 0.882 0.080 8 107366717 intron variant G/A snv 0.52 3
rs793544 0.882 0.080 3 107368152 intron variant T/C snv 0.35 3
rs807185 0.882 0.080 X 108097488 intron variant A/T snv 3
rs1326656542 0.776 0.280 13 108210293 missense variant A/T snv 4.0E-06 10
rs1805388 0.790 0.120 13 108211243 missense variant G/A snv 0.18 0.16 11