Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1198210848
rs1198210848
WRN
1 1.000 0.080 8 31058535 stop gained G/T snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs121908447
rs121908447
WRN
1 1.000 0.080 8 31147397 stop gained C/T snv 0.700 0
dbSNP: rs1244318419
rs1244318419
WRN
1 1.000 0.080 8 31076199 frameshift variant AACA/- delins 1.2E-05 1.4E-05 0.700 0
dbSNP: rs1284409960
rs1284409960
WRN
1 1.000 0.080 8 31147072 frameshift variant -/A delins 4.0E-06 0.700 0
dbSNP: rs1303126572
rs1303126572
WRN
1 1.000 0.080 8 31157509 stop gained C/T snv 7.0E-06 0.700 0
dbSNP: rs1361270203
rs1361270203
WRN
1 1.000 0.080 8 31067049 frameshift variant -/CT delins 0.700 0
dbSNP: rs1554519254
rs1554519254
WRN
1 1.000 0.080 8 31067035 frameshift variant -/AA delins 0.700 0
dbSNP: rs1554526707
rs1554526707
WRN
1 1.000 0.080 8 31111632 frameshift variant -/A delins 0.700 0
dbSNP: rs1554527775
rs1554527775
WRN
1 1.000 0.080 8 31116412 stop gained C/T snv 0.700 0
dbSNP: rs1554528411
rs1554528411
WRN
1 1.000 0.080 8 31120398 stop gained G/A snv 0.700 0
dbSNP: rs1563331288
rs1563331288
WRN
1 1.000 0.080 8 31067082 stop gained T/G snv 0.700 0
dbSNP: rs1563338837
rs1563338837
WRN
1 1.000 0.080 8 31081138 stop gained G/T snv 0.700 0
dbSNP: rs1563338855
rs1563338855
WRN
1 1.000 0.080 8 31081141 frameshift variant GA/C delins 0.700 0
dbSNP: rs1563357741
rs1563357741
WRN
1 1.000 0.080 8 31111696 stop gained C/T snv 0.700 0
dbSNP: rs1563376347
rs1563376347
WRN
1 1.000 0.080 8 31141456 stop gained T/A snv 0.700 0
dbSNP: rs1563376526
rs1563376526
WRN
1 1.000 0.080 8 31141564 stop gained T/G snv 0.700 0
dbSNP: rs1563382597
rs1563382597
WRN
1 1.000 0.080 8 31150450 frameshift variant G/- del 0.700 0
dbSNP: rs1563385391
rs1563385391
WRN
1 1.000 0.080 8 31154644 frameshift variant A/- delins 0.700 0
dbSNP: rs281865157
rs281865157
WRN
1 1.000 0.080 8 31108591 intron variant A/C;G snv 0.700 0
dbSNP: rs281865158
rs281865158
WRN
1 1.000 0.080 8 31111704 frameshift variant -/T delins 0.700 0
dbSNP: rs281865159
rs281865159
WRN
1 1.000 0.080 8 31147362 splice acceptor variant A/C snv 0.700 0
dbSNP: rs281865160
rs281865160
WRN
1 1.000 0.080 8 31150355 frameshift variant A/- delins 7.0E-06 0.700 0
dbSNP: rs369158322
rs369158322
WRN
1 1.000 0.080 8 31150454 missense variant A/C;T snv 4.0E-06 0.700 0
dbSNP: rs370324188
rs370324188
WRN
1 1.000 0.080 8 31068276 stop gained C/T snv 8.2E-06 7.0E-06 0.700 0
dbSNP: rs371538747
rs371538747
WRN
1 1.000 0.080 8 31064406 stop gained T/A;C;G snv 4.0E-06 0.700 0