Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs872071 0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs735665 0.776 0.280 11 123490689 intron variant G/A snv 0.15 8
rs13397985 0.827 0.280 2 230226508 intron variant T/C;G snv 5
rs17483466 0.827 0.280 2 111039881 intron variant A/G snv 0.15 5
rs757978 0.851 0.200 2 241431686 missense variant C/A;T snv 4.1E-06; 9.3E-02 4