Variant (rsID / SNP)
rs387906547
rs387906547 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,766,849. Clinical significance in the table: Pathogenic.
Reference-table entries
FBN1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:48766849
- Cytoband
- 15q21.1
- HGVS
- NM_000138.5(FBN1):c.3965-2A>T
- Allele change
- Silent
Associated conditions / phenotypes
Neonatal Marfan syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.