Variant (rsID / SNP)
rs281865159
rs281865159 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WRN. Location: chromosome 8, position 31,004,878. The table records no clinical significance for this variant.
Reference-table entries
WRNNot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:31004878
- Cytoband
- 8p12
- HGVS
- NM_000553.6(WRN):c.3460-2A>C
- Allele change
- Silent
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.