Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs4129267 0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs17293632 0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4