Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1167827 7 75533848 3 prime UTR variant G/A snv 0.37 5
rs17151637 8 10295572 intron variant C/G;T snv 2
rs4354968 16 76434236 intron variant T/A;C snv 2