Variant (rsID / SNP)

rs181681840

rs181681840 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,786,466. Clinical significance in the table: Benign.

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Reference-table entries

FBN1Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 15:48786466
Cytoband: 15q21.1
HGVS: NM_000138.5(FBN1):c.2678-15C>T
Allele change: Silent

Associated conditions / phenotypes

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

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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