Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
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
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs4869313 0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs57348955 0.882 0.120 16 31174561 upstream gene variant G/A;C snv 3
rs7537605 0.882 0.120 1 107800465 intron variant G/A;T snv 3
rs7679475 0.925 0.120 4 121392885 intergenic variant A/C;G snv 2
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 1
rs114846446 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs117372389 0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs17466626 0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs1270942 0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 3
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 4
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19