Variant (rsID / SNP)
rs8072510
rs8072510 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLFN13. Location: chromosome 17, position 33,772,658. The table records no clinical significance for this variant.
Reference-table entries
SLFN13Not classified
- Variant type
- stop_gained
- Chromosome / position
- 17:33772658
- HGVS
- NM_144682.6,c.42C>A,p.Tyr14*
- Allele change
- Nonsense_Y14X
Associated conditions / phenotypes
Influenza
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.