Variant (rsID / SNP)
rs281865158
rs281865158 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WRN. Location: chromosome 8, position 30,969,220. The table records no clinical significance for this variant.
Reference-table entries
WRNNot classified
- Variant type
- Duplication
- Chromosome / position
- 8:30969220
- Cytoband
- 8p12
- HGVS
- NM_000553.6(WRN):c.2179dup (p.Cys727fs)
Associated conditions / phenotypes
Werner syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.