Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs4625 0.716 0.280 3 49534707 3 prime UTR variant A/G snv 0.30 17
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 15
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 15
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 15
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 15
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 15
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 15
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14