Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
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
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
rs12928404 0.724 0.240 16 28835925 splice region variant T/C snv 0.44 0.45 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
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs602662 0.716 0.280 19 48703728 missense variant G/A snv 0.40 0.47 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
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
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs114846446 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs117372389 0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs11741255 0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14