Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35628 1.000 0.080 16 16077249 intron variant A/G snv 0.13 1
rs3888565 1.000 0.080 16 16089188 intron variant G/A snv 0.25 1
rs4148353 1.000 0.080 16 16077291 intron variant G/A;T snv 1