Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554754182 0.827 0.200 9 105606576 intron variant G/T snv 5
rs746763506 0.851 0.160 9 105604452 stop gained C/T snv 8.0E-06 7.0E-06 4
rs398123555 0.882 0.160 9 105620050 frameshift variant A/-;AA delins 3
rs119463990 0.925 0.120 9 105596631 stop gained C/T snv 1.6E-05 7.0E-06 2
rs119464998 0.925 0.120 9 105620001 missense variant A/G snv 2.8E-05 2.1E-05 2
rs1309132512 0.925 0.120 9 105575074 frameshift variant G/- del 7.0E-06 2
rs267606814 0.925 0.120 9 105617967 stop gained C/G;T snv 2.0E-05 2
rs398123557 0.925 0.120 9 105604483 frameshift variant -/T delins 2
rs750176716 0.925 0.120 9 105619989 frameshift variant T/- delins 2.0E-05 2
rs775681117 1.000 0.120 19 46756129 missense variant G/C snv 1
rs1057516258 1.000 0.120 9 105604272 frameshift variant A/- delins 1
rs1057516966 1.000 0.120 9 105607941 frameshift variant C/- del 1
rs1057517160 1.000 0.120 9 105607829 frameshift variant CAGC/- del 1
rs1180986256 1.000 0.120 9 105575031 start lost AAT/- delins 4.0E-06 7.0E-06 1
rs119463991 1.000 0.120 9 105601325 stop gained C/T snv 1.4E-05 1
rs119464997 1.000 0.120 9 105604354 missense variant C/A;T snv 8.0E-06 1
rs1554748292 1.000 0.120 9 105596596 splice acceptor variant A/G snv 1
rs1554752805 1.000 0.120 9 105604213 splice acceptor variant A/G snv 1
rs1554761310 1.000 0.120 9 105619988 frameshift variant G/- del 1
rs1554761402 1.000 0.120 9 105620018 frameshift variant AT/- del 1
rs1554761462 1.000 0.120 9 105620062 splice donor variant G/A snv 1
rs1554766808 1.000 0.120 9 105635049 splice acceptor variant A/G snv 1
rs370819786 1.000 0.120 9 105607952 splice donor variant G/A;T snv 1
rs537001725 1.000 0.120 9 105604256 stop gained C/A;T snv 2.4E-05; 8.0E-06 1
rs557699482 1.000 0.120 9 105635050 splice acceptor variant G/A;C;T snv 4.0E-06 1