Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs12243326 0.925 0.160 10 113029056 intron variant T/C snv 0.27 5
rs7936247 1.000 0.040 11 92956866 intergenic variant G/T snv 0.37 5
rs2877716 3 123375604 intron variant T/C snv 0.76 4
rs853789 2 168944978 intron variant A/G;T snv 0.75 4
rs17271340 15 62055686 intron variant C/T snv 0.33 2
rs2042608 15 61940181 intron variant C/A snv 0.48 2