Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1284409960
WRN
1.000 0.080 8 31147072 frameshift variant -/A delins 4.0E-06 1
rs1554526707
WRN
1.000 0.080 8 31111632 frameshift variant -/A delins 1
rs587776621
WRN
1.000 0.080 8 31157462 frameshift variant -/A delins 1
rs1554519254
WRN
1.000 0.080 8 31067035 frameshift variant -/AA delins 1
rs878854136
WRN
1.000 0.080 8 31120338 frameshift variant -/AT delins 1
rs1361270203
WRN
1.000 0.080 8 31067049 frameshift variant -/CT delins 1
rs747587698
WRN
1.000 0.080 8 31064304 frameshift variant -/G delins 1
rs281865158
WRN
1.000 0.080 8 31111704 frameshift variant -/T delins 1
rs1563385391
WRN
1.000 0.080 8 31154644 frameshift variant A/- delins 1
rs281865160
WRN
1.000 0.080 8 31150355 frameshift variant A/- delins 7.0E-06 1
rs878854131
WRN
1.000 0.080 8 31081190 frameshift variant A/- delins 2.1E-05 1
rs778872619
WRN
1.000 0.080 8 31143616 frameshift variant A/-;AA delins 1
rs878854133
WRN
1.000 0.080 8 31058455 frameshift variant A/-;AA delins 1.4E-05 1
rs281865159
WRN
1.000 0.080 8 31147362 splice acceptor variant A/C snv 1
rs281865157
WRN
1.000 0.080 8 31108591 intron variant A/C;G snv 1
rs369158322
WRN
1.000 0.080 8 31150454 missense variant A/C;T snv 4.0E-06 1
rs1563341296
WRN
1.000 0.080 8 31085164 splice acceptor variant A/G snv 1
rs267607008
WRN
1.000 0.080 8 31064962 missense variant A/G snv 1
rs121908448
WRN
1.000 0.080 8 31090843 missense variant A/T snv 1
rs387906337
WRN
1.000 0.080 8 31064934 missense variant A/T snv 1
rs776785728
WRN
1.000 0.080 8 31065058 frameshift variant AA/- delins 6.4E-05 2.1E-05 1
rs1244318419
WRN
1.000 0.080 8 31076199 frameshift variant AACA/- delins 1.2E-05 1.4E-05 1
rs748860208
WRN
1.000 0.080 8 31141490 frameshift variant AACA/- delins 5.6E-05 1
rs1383589957
WRN
1.000 0.080 8 31111628 frameshift variant AC/- delins 4.0E-06 2.8E-05 1
rs759972548
WRN
1.000 0.080 8 31141495 frameshift variant AG/- delins 1.4E-05 1