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 18
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs4148325 0.851 0.080 2 233764663 intron variant C/T snv 0.36 11
rs17863787 0.925 0.040 2 233702448 intron variant T/G snv 0.30 9
rs929596 0.925 0.040 2 233765830 intron variant A/G snv 0.32 9
rs3755319 0.925 0.120 2 233758936 intron variant A/C;G;T snv 8
rs4124874 0.851 0.120 2 233757013 intron variant T/A;G snv 8
rs1875263 1.000 2 233716976 intron variant C/G;T snv 7
rs4663969 1.000 2 233746667 intron variant C/A;T snv 6
rs10203853 1.000 0.080 2 233778772 intron variant A/G;T snv 5
rs10929251 1.000 0.080 2 233637583 intron variant A/G snv 0.13 5
rs11892031 0.882 0.120 2 233656637 intron variant A/C;T snv 5
rs17864678 1.000 0.080 2 233635964 intron variant T/A snv 5.6E-03 5
rs4148326 0.925 0.080 2 233764816 intron variant T/C snv 0.49 5
rs4149081 1.000 0.040 12 21225087 intron variant G/A snv 0.18 5
rs4363657 12 21215788 intron variant T/C snv 0.18 5
rs6728940 1.000 0.080 2 233780518 intron variant G/A snv 0.26 5
rs10178992 2 233749231 intron variant T/A snv 0.37 4
rs10179091 2 233749337 intron variant T/C snv 0.49 4
rs10929302 2 233757136 intron variant G/A snv 0.30 4
rs11045879 1.000 0.120 12 21229685 intron variant T/C snv 0.18 4
rs11891311 2 233730664 intron variant G/A snv 0.42 4
rs1550532 2 233356202 intron variant C/G snv 0.75 4
rs17862875 2 233740656 intron variant G/A snv 0.30 4
rs2741045 2 233671494 intron variant C/T snv 0.22 4