Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3130215 0.882 0.240 6 33107186 intron variant A/G snv 0.69 3
rs2064478 0.925 0.200 6 33104489 intron variant C/T snv 0.28 2
rs2064476 0.925 0.200 6 33105545 intron variant A/G snv 0.37 2
rs4282438 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 2
rs3117231 1.000 0.120 6 33107131 intron variant A/G snv 0.31 1
rs3128927 1.000 0.120 6 33106511 intron variant C/G;T snv 1