Variant (rsID / SNP)

rs267606798

rs267606798 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,758,022. Clinical significance in the table: Likely pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FBN1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 15:48758022
Cytoband: 15q21.1
HGVS: NM_000138.5(FBN1):c.4781G>A (p.Gly1594Asp)
Allele change: Missense_G1594D

Associated conditions / phenotypes

Stiff skin syndrome|Marfan syndrome

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.