Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1567713938 1.000 0.080 17 3658090 frameshift variant -/A delins 1
rs745365232 1.000 0.080 17 3656543 stop gained CA/- delins 1.2E-05 1
rs752919200 1.000 0.080 17 3658151 frameshift variant -/A delins 4.0E-06 1
rs763089013 1.000 0.080 17 3658057 stop gained G/A;C snv 1.2E-05 1
rs908965524 1.000 0.080 17 3659928 missense variant G/T snv 1
rs922106812 1.000 0.080 17 3659866 missense variant G/C snv 1
rs955833453 1.000 0.080 17 3655103 splice donor variant T/C snv 4.0E-06 1
rs1555558034 1.000 0.080 17 3640187 splice acceptor variant G/A snv 1
rs1555558078 1.000 0.080 17 3640226 frameshift variant C/- del 1
rs1555558099 1.000 0.080 17 3640243 frameshift variant C/- delins 1
rs1555558116 1.000 0.080 17 3640268 splice donor variant G/A snv 1
rs1555561049 1.000 0.080 17 3648932 splice donor variant G/A snv 1
rs1567695026 1.000 0.080 17 3640264 stop gained TG/- delins 1
rs1057516296 1.000 0.080 17 3655021 frameshift variant A/- delins 1
rs1212133760 1.000 0.080 17 3659898 missense variant G/A snv 4.0E-06 1
rs121908124 1.000 0.080 17 3655055 stop gained G/T snv 1
rs121908126 1.000 0.080 17 3656531 missense variant G/A snv 1
rs1327959008 1.000 0.080 17 3656779 missense variant A/G snv 4.0E-06 1
rs1555562830 1.000 0.080 17 3655090 frameshift variant ATCA/- delins 1
rs1555563010 1.000 0.080 17 3655342 missense variant A/G snv 1
rs1555563446 1.000 0.080 17 3656543 missense variant A/G snv 1
rs1555563568 1.000 0.080 17 3656706 frameshift variant G/- del 1
rs1555563658 1.000 0.080 17 3656795 splice donor variant G/- delins 1
rs1555563982 1.000 0.080 17 3658015 frameshift variant -/CG delins 1
rs1555564588 1.000 0.080 17 3659857 splice acceptor variant G/A snv 1