Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3217810 0.776 0.080 12 4279105 intron variant C/T snv 8.7E-02 10
rs3217874 0.776 0.080 12 4291642 intron variant C/T snv 0.37 10
rs3217901 0.790 0.080 12 4296223 intron variant A/G snv 0.35 9