Variant (rsID / SNP)
rs2981582
rs2981582 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGFR2. Location: chromosome 10, position 123,352,317. Clinical significance in the table: Benign.
Reference-table entries
FGFR2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 10:123352317
- Cytoband
- 10q26.13
- HGVS
- NM_000141.5(FGFR2):c.109+906T>C
- Allele change
- Silent
Associated conditions / phenotypes
FGFR2 related craniosynostosis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.