Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs1935057 1.000 0.040 13 105458997 upstream gene variant G/A snv 0.51 1
rs3916967 0.882 0.040 13 105464999 intron variant T/C snv 0.32 3
rs2391191 0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs1046943 1.000 0.040 6 109462738 3 prime UTR variant A/G snv 0.52 3
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1200746244 0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs781140785 0.925 0.040 7 150952801 missense variant C/T snv 1.2E-05 4.2E-05 2
rs2619522 0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs953038635 0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs2197414 1.000 0.040 5 161681878 intron variant G/A;C snv 1
rs4921195 1.000 0.040 5 161684582 intron variant C/A;T snv 1
rs13188991 1.000 0.040 5 161685998 synonymous variant G/A;C snv 0.19 0.18 1
rs11956731 1.000 0.040 5 161700816 intron variant C/A;T snv 1
rs78247304 0.925 0.040 2 162446391 missense variant C/T snv 7.6E-05 6.4E-04 2
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
rs5326 0.851 0.160 5 175443193 5 prime UTR variant C/T snv 0.15 6
rs7619173 1.000 0.040 3 181279171 intron variant C/T snv 0.49 1
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs11636988 1.000 0.040 15 26577667 intron variant G/A snv 0.43 1
rs8024256 1.000 0.040 15 26584374 intron variant A/G snv 0.61 1