Variant (rsID / SNP)
rs6056
rs6056 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGB. Location: chromosome 4, position 155,488,821. Clinical significance in the table: Benign.
Reference-table entries
FGBBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:155488821
- Cytoband
- 4q31.3
- HGVS
- NM_005141.5(FGB):c.567C>T (p.Ser189=)
- Allele change
- Synonymous_S130S
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.