Variant (rsID / SNP)
rs121918490
rs121918490 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGFR2. Location: chromosome 10, position 123,276,856. Clinical significance in the table: Pathogenic.
Reference-table entries
FGFR2Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:123276856
- Cytoband
- 10q26.13
- HGVS
- NM_000141.5(FGFR2):c.1061C>G (p.Ser354Cys)
- Allele change
- Missense_S354C
Associated conditions / phenotypes
Crouzon syndrome|FGFR2 related craniosynostosis|Inborn genetic diseases|See cases
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.