Variant (rsID / SNP)
rs397515769
rs397515769 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,788,303. Clinical significance in the table: Pathogenic.
Reference-table entries
FBN1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 15:48788303
- Cytoband
- 15q21.1
- HGVS
- NM_000138.5(FBN1):c.2412_2413del (p.Thr804_Cys805insTer)
Associated conditions / phenotypes
Marfan syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.