Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs912322 1.000 0.080 13 109155938 intron variant A/G snv 0.23 1
rs150813880 1.000 0.080 13 109140829 synonymous variant G/A snv 2.6E-02 1.9E-02 1
rs17393344 1.000 0.080 13 108821598 intron variant G/A snv 2.4E-02 1