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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs11154178 0.807 0.240 6 123540174 intron variant T/A;C snv 7
rs28485846 0.807 0.240 8 35265058 intron variant C/T snv 5.1E-02 7
rs3761980 0.807 0.240 6 36026129 upstream gene variant A/G snv 0.14 7
rs71597855 0.807 0.240 4 53790270 intron variant G/A snv 2.5E-02 7
rs80028505 0.807 0.240 6 36030611 intron variant C/G;T snv 7
rs689 0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 3
rs9273368 0.882 0.120 6 32658698 upstream gene variant G/A snv 0.23 3
rs7111341 0.925 0.120 11 2191936 regulatory region variant C/T snv 0.29 2
rs7202877 0.882 0.160 16 75213347 intergenic variant T/C;G snv 2