Variant (rsID / SNP)
rs34690599
rs34690599 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HBB. Location: chromosome 11, position 5,247,062. Clinical significance in the table: Pathogenic.
Reference-table entries
HBBPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:5247062
- Cytoband
- 11p15.4
- HGVS
- NM_000518.5(HBB):c.316-106C>G
- Allele change
- Silent
Associated conditions / phenotypes
Beta-plus-thalassemia|beta Thalassemia|9 conditions|Hb SS disease|Dominant beta-thalassemia|Beta-thalassemia HBB/LCRB
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.