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Variant (rsID / SNP)

rs111687884

FBN1

rs111687884 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,829,901. Clinical significance in the table: Pathogenic.

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Reference-table entries

FBN1Pathogenic
Clinical significance (as recorded)
Pathogenic
Variant type
single nucleotide variant
Chromosome / position
15:48829901
Cytoband
15q21.1
HGVS
NM_000138.5(FBN1):c.643C>T (p.Arg215Ter)
Allele change
Nonsense_R215X

Associated conditions / phenotypes

Marfan syndrome|Cardiovascular phenotype|Familial thoracic aortic aneurysm and aortic dissection|Marfan syndrome|Progeroid and marfanoid aspect-lipodystrophy syndrome

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.