Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs941823 0.827 0.120 13 40439840 intron variant T/C snv 0.77 6
rs17061048 1.000 0.040 13 40258875 intron variant T/A snv 3.4E-02 2
rs915286 1.000 0.040 13 40121855 intron variant G/A;C snv 2