Variant (rsID / SNP)
rs35456885
rs35456885 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HBB. Location: chromosome 11, position 5,248,044. Clinical significance in the table: Likely benign.
Reference-table entries
HBBLikely benign
- Clinical significance (as recorded)
- Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:5248044
- Cytoband
- 11p15.4
- HGVS
- NM_000518.5(HBB):c.93-15T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.