Variant (rsID / SNP)
rs34218908
rs34218908 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HBB. Location: chromosome 11, position 5,247,896. Clinical significance in the table: Likely pathogenic.
Reference-table entries
HBBLikely pathogenic
- Clinical significance (as recorded)
- Likely pathogenic
- Variant type
- Deletion
- Chromosome / position
- 11:5247896
- Cytoband
- 11p15.4
- HGVS
- NM_000518.5(HBB):c.226del (p.Leu76fs)
Associated conditions / phenotypes
beta Thalassemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.