Variant (rsID / SNP)
rs2066865
rs2066865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGG. Location: chromosome 4, position 155,525,276. Clinical significance in the table: Benign.
Reference-table entries
FGGBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:155525276
- Cytoband
- 4q32.1
- HGVS
- NM_000509.5(FGG):c.*216C>T
Associated conditions / phenotypes
Congenital afibrinogenemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.