Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7203560 1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 6
rs117747069 16 120077 intron variant G/C snv 2.5E-02 4
rs2238368 16 120329 intron variant C/T snv 0.36 3