Variant (rsID / SNP)
rs63750128
rs63750128 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HBB. Location: chromosome 11, position 5,247,967. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
HBBPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- Deletion
- Chromosome / position
- 11:5247967
- Cytoband
- 11p15.4
- HGVS
- NM_000518.5(HBB):c.155del (p.Pro52fs)
Associated conditions / phenotypes
beta Thalassemia|Hemoglobinopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.