Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1163944538 0.641 0.560 17 75494905 frameshift variant -/A delins 4.0E-06 73
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs587783446 0.763 0.280 8 60850546 stop gained C/T snv 19
rs112550005 0.742 0.240 15 48425829 stop gained G/A snv 18
rs727503057 0.708 0.280 15 48505106 missense variant G/A snv 7.0E-06 16
rs121918327 0.776 0.240 4 122742955 stop gained C/T snv 2.8E-05 1.4E-05 12
rs869312685 0.807 0.240 3 4815135 missense variant G/A;C snv 11
rs397515789 0.776 0.240 15 48488112 splice donor variant C/A;T snv 10
rs121918461 0.827 0.240 12 112450362 missense variant A/C;G;T snv 8
rs886039902 0.851 0.360 16 89284130 frameshift variant TTTTT/-;T;TTTT delins 6
rs775394591 0.851 0.120 13 38784727 inframe deletion TCT/- delins 2.8E-05 5
rs869312741 0.882 0.080 19 43747509 frameshift variant GG/- delins 5
rs869312742 0.882 0.080 19 43744768 splice region variant T/C snv 5