Variant (rsID / SNP)
rs80334351
rs80334351 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BBS4. Location: chromosome 15, position 73,009,208. Clinical significance in the table: Benign.
Reference-table entries
BBS4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:73009208
- Cytoband
- 15q24.1
- HGVS
- NM_033028.5(BBS4):c.405+17C>T
- Allele change
- Silent
Associated conditions / phenotypes
Bardet-Biedl syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.