Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs887829 0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs11891311 2 233730664 intron variant G/A snv 0.42 4
rs1550532 2 233356202 intron variant C/G snv 0.75 4
rs4149081 1.000 0.040 12 21225087 intron variant G/A snv 0.18 4
rs10167119 2 233680666 intron variant T/C snv 0.34 3
rs10168155 2 233688190 intron variant C/T snv 0.39 3
rs10168333 2 233688342 intron variant C/T snv 0.39 3
rs10171367 2 233689021 intron variant C/A;G snv 3
rs10175809 2 233688219 intron variant T/A snv 0.39 3
rs10178992 2 233749231 intron variant T/A snv 0.37 3
rs10179091 2 233749337 intron variant T/C snv 0.49 3
rs10179094 2 233689179 intron variant T/A snv 0.34 3
rs10197460 2 233680544 intron variant G/T snv 0.34 3
rs10929302 2 233757136 intron variant G/A snv 0.30 3
rs11045879 1.000 0.120 12 21229685 intron variant T/C snv 0.18 3
rs11680450 2 233688837 intron variant T/A;C snv 3
rs11694406 2 233423164 intron variant G/A snv 0.12 3
rs11892031 0.882 0.120 2 233656637 intron variant A/C;T snv 3
rs11902131 2 233685623 intron variant C/T snv 0.39 3
rs13002774 2 233685060 intron variant G/A;T snv 3
rs13015720 2 233692353 intron variant G/A snv 0.39 3
rs1604144 2 233697189 intron variant C/T snv 0.33 3
rs17862866 2 233702266 intron variant A/G;T snv 3
rs17862875 2 233740656 intron variant G/A snv 0.30 3
rs17863787 0.925 0.040 2 233702448 intron variant T/G snv 0.30 3