Variant (rsID / SNP)

rs2267989

rs2267989 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBLN5. Location: chromosome 14, position 92,339,850. The table records no clinical significance for this variant.

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Reference-table entries

FBLN5Not classified

Variant type: missense_variant
Chromosome / position: 14:92339850
HGVS: NM_001384160.1,c.1355C>T,p.Pro452Leu
Allele change: Silent

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.