Variant (rsID / SNP)
rs11574158
rs11574158 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to WRN. Location: chromosome 8, position 30,891,353. Clinical significance in the table: Benign.
Reference-table entries
WRNBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:30891353
- Cytoband
- 8p12
- HGVS
- NM_000553.6(WRN):c.-213G>A
- 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.