Variant (rsID / SNP)
rs121918499
rs121918499 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGFR2. Location: chromosome 10, position 123,279,562. Clinical significance in the table: Pathogenic.
Reference-table entries
FGFR2Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:123279562
- Cytoband
- 10q26.13
- HGVS
- NM_000141.5(FGFR2):c.870G>C (p.Trp290Cys)
- Allele change
- Missense_W290C
Associated conditions / phenotypes
Pfeiffer syndrome|Squamous cell lung carcinoma|Aural atresia, congenital
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.