Variant (rsID / SNP)
rs34889882
rs34889882 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HBB. Location: chromosome 11, position 5,248,234. Clinical significance in the table: Pathogenic.
Reference-table entries
HBBPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 11:5248234
- Cytoband
- 11p15.4
- HGVS
- NM_000518.5(HBB):c.17_18del (p.Pro6fs)
Associated conditions / phenotypes
Beta zero thalassemia|beta Thalassemia|Hb SS disease|9 conditions
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.