Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806 0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs886040971 0.683 0.280 8 115604339 stop gained G/A;T snv 56
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs1559155954 0.851 0.200 2 219568211 frameshift variant -/A delins 9