Variant (rsID / SNP)
rs9509843
rs9509843 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGF9. Location: chromosome 13, position 22,276,070. Clinical significance in the table: Benign.
Reference-table entries
FGF9Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 13:22276070
- Cytoband
- 13q12.11
- HGVS
- NM_002010.3(FGF9):c.*496C>T
- Allele change
- Silent
Associated conditions / phenotypes
Multiple synostoses syndrome 3
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.