Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35188965 5 1104823 intron variant C/G;T snv 12
rs1569419 1 3080038 intron variant T/C snv 0.73 5
rs78909033 2 240571486 intron variant G/A snv 9.2E-02 5