Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs984456066 12 14460956 missense variant G/A snv 1
rs12979618 19 38269930 intron variant G/T snv 0.27 1