Variant (rsID / SNP)
rs1044291
rs1044291 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FGB. Location: chromosome 4, position 155,493,352. Clinical significance in the table: Benign.
Reference-table entries
FGBBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:155493352
- Cytoband
- 4q31.3
- HGVS
- NM_005141.5(FGB):c.*1550C>T
- Allele change
- Silent
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.