Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11193085 10 106873848 intron variant G/A snv 8.8E-02 3
rs12247406 10 106996746 intron variant G/A snv 1.3E-02 3
rs11813704 10 107102114 intron variant G/T snv 3.1E-02 2
rs7910584 1.000 0.040 10 106607970 intron variant C/A snv 0.65 1
rs2756231 10 106706654 intron variant C/T snv 0.98 0.97 1