Variant (rsID / SNP)
rs886041859
rs886041859 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,725,177. Clinical significance in the table: Pathogenic.
Reference-table entries
FBN1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:48725177
- Cytoband
- 15q21.1
- HGVS
- NM_000138.5(FBN1):c.6625G>T (p.Glu2209Ter)
- Allele change
- Nonsense_E2209X
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.