Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6091189 0.776 0.080 20 50639748 intron variant C/T snv 0.25 10
rs914458 0.925 0.080 20 50594416 intron variant G/C snv 0.23 2
rs1060402 20 50588558 intron variant G/A snv 0.45 1
rs117246187 20 50690397 intron variant A/G snv 5.7E-02 1