Variant (rsID / SNP)

rs778181932

rs778181932 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FBN1. Location: chromosome 15, position 48,780,628. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

FBN1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 15:48780628
Cytoband: 15q21.1
HGVS: NM_000138.5(FBN1):c.3145G>T (p.Gly1049Cys)
Allele change: Missense_G1049C

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.