Variant (rsID / SNP)
rs33944208
rs33944208 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HBB. Location: chromosome 11, position 5,248,389. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
HBBPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:5248389
- Cytoband
- 11p15.4
- HGVS
- NM_000518.5(HBB):c.-138C>T
Associated conditions / phenotypes
Beta-plus-thalassemia|beta Thalassemia|Hemoglobinopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.