Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11642387 16 6703238 intron variant A/G snv 6.7E-02 1
rs11643447 16 6649260 intron variant A/G;T snv 1
rs2058527 16 6654748 intron variant T/G snv 0.75 1
rs9302817 16 6113935 intron variant T/A;G snv 1