Variant (rsID / SNP)

rs187177496

rs187177496 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,766,755. Clinical significance in the table: Uncertain significance.

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Reference-table entries

FBN1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 15:48766755
Cytoband: 15q21.1
HGVS: NM_000138.5(FBN1):c.4057G>A (p.Gly1353Arg)
Allele change: Missense_G1353W

Associated conditions / phenotypes

Inborn genetic diseases|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.