Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000879 2 218439407 intron variant G/A snv 4.1E-02 3
rs6726798 2 218436132 intron variant A/C snv 0.94 3
rs6717434 2 218423414 intron variant A/G;T snv 1