Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs78534766 0.827 0.080 16 50301163 missense variant C/A snv 4.3E-03 3.6E-03 7