Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs148636776 0.790 0.280 12 111447491 missense variant G/A snv 1.5E-04 2.4E-04 18
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10
rs2681472 0.882 0.080 12 89615182 intron variant A/G snv 0.14 9
rs1004467 0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 8
rs16964543 1.000 0.080 19 30694303 intron variant T/C snv 0.32 2