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Variant (rsID / SNP)

rs113905529

FBN1

rs113905529 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,888,525. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

FBN1Pathogenic
Clinical significance (as recorded)
Pathogenic/Likely pathogenic
Variant type
single nucleotide variant
Chromosome / position
15:48888525
Cytoband
15q21.1
HGVS
NM_000138.5(FBN1):c.493C>T (p.Arg165Ter)
Allele change
Nonsense_R165X

Associated conditions / phenotypes

Marfan syndrome|Marfan syndrome|Familial thoracic aortic aneurysm and aortic dissection|Familial thoracic aortic aneurysm and aortic dissection|Isolated thoracic aortic aneurysm

Public references

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