Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs17622378 0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs2066844 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 5
rs449454 0.925 0.080 5 142153497 3 prime UTR variant A/G snv 0.65 0.68 3