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Variant (rsID / SNP)

rs199665922

FBN2

rs199665922 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN2. Location: chromosome 5, position 127,664,405. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

FBN2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
5:127664405
Cytoband
5q23.3
HGVS
NM_001999.4(FBN2):c.4454A>G (p.Asp1485Gly)
Allele change
Missense_D1485G

Associated conditions / phenotypes

Cardiovascular phenotype|Congenital contractural arachnodactyly|Connective tissue disorder

Public references

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