Variant (rsID / SNP)

rs9509841

rs9509841 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGF9. Location: chromosome 13, position 22,275,394. Clinical significance in the table: Benign.

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Reference-table entries

FGF9Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:22275394
Cytoband: 13q12.11
HGVS: NM_002010.3(FGF9):c.447A>G (p.Ser149=)
Allele change: Synonymous_S149S

Associated conditions / phenotypes

Multiple synostoses syndrome 3

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.