Variant (rsID / SNP)

rs397515802

rs397515802 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,764,862. 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: 15:48764862
Cytoband: 15q21.1
HGVS: NM_000138.5(FBN1):c.4222T>C (p.Cys1408Arg)
Allele change: Missense_C1408R

Associated conditions / phenotypes

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

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.