Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2004640 0.662 0.520 7 128938247 splice donor variant T/G snv 0.52 26
rs113993959 0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs74597325 0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 18
rs149989682 0.790 0.240 16 2317763 missense variant T/A;C snv 2.3E-03 10
rs8182352 0.827 0.160 17 5651667 intergenic variant T/C snv 0.44 5
rs876657633 1.000 0.120 16 2300001 splice donor variant GCACCTT/TGG delins 1