Variant (rsID / SNP)
rs61746008
rs61746008 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,704,816. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
FBN1Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 15:48704816
- Cytoband
- 15q21.1
- HGVS
- NM_000138.5(FBN1):c.8176C>T (p.Arg2726Trp)
- Allele change
- Missense_R2726W
Associated conditions / phenotypes
Marfan syndrome|Familial thoracic aortic aneurysm and aortic dissection|Acromicric dysplasia|Geleophysic dysplasia|Weill-Marchesani syndrome|Ectopia lentis 1, isolated, autosomal dominant|Stiff skin syndrome|Inborn genetic diseases|Familial thoracic aortic aneurysm and aortic dissection|Marfan syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.