Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs7632505 0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs72661131 0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs4636297 0.724 0.360 9 136670698 intron variant A/G snv 0.67 0.65 14
rs5744174 0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs1799987 0.763 0.200 3 46370444 intron variant A/G snv 0.49 10
rs3774261 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs2229116 0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs2266780 0.827 0.280 1 171114102 missense variant A/G snv 0.15 0.14 9
rs2288904 0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs2359612 0.851 0.120 16 31092475 intron variant A/G snv 0.66 7
rs2986017 0.851 0.120 10 103458495 missense variant A/G snv 0.79 0.80 6
rs34166473
HBD
0.827 0.320 11 5234513 5 prime UTR variant A/G snv 7.0E-06 6
rs73885319 0.851 0.120 22 36265860 missense variant A/G snv 1.6E-02 6.6E-02 6
rs17114036 0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs275653 0.882 0.120 3 148697758 upstream gene variant A/G snv 0.20 5