Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115460205 1.000 0.080 4 161890417 intron variant C/T snv 4.7E-02 3
rs17536732 1.000 0.080 4 161903214 intron variant G/T snv 4.7E-02 3