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
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs606231435 0.827 0.240 19 41970539 missense variant C/T snv 18