Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1744297 14 104102135 intron variant T/C snv 0.86 12
rs3815652 0.925 0.160 7 33873792 intron variant C/T snv 0.19 3
rs75444260 7 635944 intron variant A/G snv 8.5E-02 3