Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs12914385 0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs56113850 0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs13141641 1.000 0.040 4 144585304 intron variant T/C snv 0.32 6
rs9788721 1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs138544659 1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs55958997 1.000 0.040 15 78623530 upstream gene variant C/A snv 0.32 5
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 5
rs2316205 19 40840863 non coding transcript exon variant T/C snv 0.40 4
rs113029345 19 40864271 intron variant T/C snv 3