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Variant (rsID / SNP)

rs9682

FBLN1

rs9682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBLN1. Location: chromosome 22, position 45,937,149. The table records no clinical significance for this variant.

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Reference-table entries

FBLN1Not classified
Variant type
synonymous_variant
Chromosome / position
22:45937149
HGVS
NM_006486.3,c.963C>T,p.Ile321Ile
Allele change
Synonymous_I321I

Public references

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