Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs956572 0.742 0.280 18 63153338 intron variant A/G snv 0.65 11
rs2619522 0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs5326 0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs1046943 1.000 0.040 6 109462738 3 prime UTR variant A/G snv 0.52 3
rs3916967 0.882 0.040 13 105464999 intron variant T/C snv 0.32 3
rs11637898 0.925 0.040 15 92409620 intron variant G/A snv 0.43 2
rs17026688 1.000 0.040 3 30845325 intron variant C/T snv 9.3E-03 2
rs11001178 1.000 0.040 10 74842047 intron variant T/C;G snv 1
rs11636988 1.000 0.040 15 26577667 intron variant G/A snv 0.43 1
rs11956731 1.000 0.040 5 161700816 intron variant C/A;T snv 1
rs12547858 1.000 0.040 8 32629535 intron variant C/T snv 0.15 1
rs1475196 1.000 0.040 13 46881488 intron variant A/C snv 1.4E-03 1
rs17110566 1.000 0.040 12 71972867 intron variant G/A snv 3.9E-02 1
rs1935057 1.000 0.040 13 105458997 upstream gene variant G/A snv 0.51 1
rs2197414 1.000 0.040 5 161681878 intron variant G/A;C snv 1
rs2217887 1.000 0.040 14 79417482 intron variant T/C snv 0.31 1
rs3757933 1.000 0.040 8 32747325 intron variant G/A snv 0.23 1
rs3815762 1.000 0.040 5 170788816 intron variant T/A snv 0.11 1
rs4868029 1.000 0.040 5 170790498 intron variant C/T snv 0.36 1
rs4921195 1.000 0.040 5 161684582 intron variant C/A;T snv 1