Variant (rsID / SNP)
rs34856846
rs34856846 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HBB. Location: chromosome 11, position 5,248,216. Clinical significance in the table: Pathogenic.
Reference-table entries
HBBPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 11:5248216
- Cytoband
- 11p15.4
- HGVS
- NM_000518.5(HBB):c.36del (p.Thr13fs)
Associated conditions / phenotypes
Beta zero thalassemia|Hemoglobinopathy|beta Thalassemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.