Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2302254 0.752 0.240 17 51153539 5 prime UTR variant C/T snv 0.22 15
rs2303428 0.776 0.240 2 47476361 splice region variant T/A;C;G snv 4.0E-06; 0.12 9
rs4648068 0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs1801200 0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs6917
PHB
0.790 0.200 17 49404181 3 prime UTR variant G/A snv 0.16 7