Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs369158322
WRN
1.000 0.080 8 31150454 missense variant A/C;T snv 4.0E-06 1
rs371538747
WRN
1.000 0.080 8 31064406 stop gained T/A;C;G snv 4.0E-06 1
rs121908447
WRN
1.000 0.080 8 31147397 stop gained C/T snv 1
rs121908448
WRN
1.000 0.080 8 31090843 missense variant A/T snv 1
rs1303126572
WRN
1.000 0.080 8 31157509 stop gained C/T snv 7.0E-06 1
rs1304645785
WRN
1.000 0.080 8 31090532 missense variant G/A snv 1
rs1361270203
WRN
1.000 0.080 8 31067049 frameshift variant -/CT delins 1
rs1554519254
WRN
1.000 0.080 8 31067035 frameshift variant -/AA delins 1
rs1554519449
WRN
1.000 0.080 8 31068326 splice donor variant GGTA/- delins 1
rs1554526707
WRN
1.000 0.080 8 31111632 frameshift variant -/A delins 1
rs1554527775
WRN
1.000 0.080 8 31116412 stop gained C/T snv 1
rs1554528411
WRN
1.000 0.080 8 31120398 stop gained G/A snv 1
rs1563331288
WRN
1.000 0.080 8 31067082 stop gained T/G snv 1
rs1563338837
WRN
1.000 0.080 8 31081138 stop gained G/T snv 1
rs1563338855
WRN
1.000 0.080 8 31081141 frameshift variant GA/C delins 1
rs1563341296
WRN
1.000 0.080 8 31085164 splice acceptor variant A/G snv 1
rs1563357741
WRN
1.000 0.080 8 31111696 stop gained C/T snv 1
rs1563376347
WRN
1.000 0.080 8 31141456 stop gained T/A snv 1
rs1563376526
WRN
1.000 0.080 8 31141564 stop gained T/G snv 1
rs1563376793
WRN
1.000 0.080 8 31141776 splice donor variant G/C snv 1
rs1563382597
WRN
1.000 0.080 8 31150450 frameshift variant G/- del 1
rs1563385391
WRN
1.000 0.080 8 31154644 frameshift variant A/- delins 1
rs267607008
WRN
1.000 0.080 8 31064962 missense variant A/G snv 1
rs281865157
WRN
1.000 0.080 8 31108591 intron variant A/C;G snv 1
rs281865158
WRN
1.000 0.080 8 31111704 frameshift variant -/T delins 1