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Variant (rsID / SNP)

rs4804264

FBN3

rs4804264 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN3. Location: chromosome 19, position 8,176,919. The table records no clinical significance for this variant.

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Reference-table entries

FBN3Not classified
Variant type
synonymous_variant
Chromosome / position
19:8176919
HGVS
NM_001321431.2,c.3903G>A,p.Pro1301Pro
Allele change
Synonymous_P1301P

Public references

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