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Variant (rsID / SNP)

rs137854468

FBN1

rs137854468 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,779,593. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FBN1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
15:48779593
Cytoband
15q21.1
HGVS
NM_000138.5(FBN1):c.3379G>A (p.Gly1127Ser)
Allele change
Missense_G1127S

Associated conditions / phenotypes

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

Public references

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