Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs9679162 0.882 0.120 2 31024648 intron variant G/T snv 0.48 4