Variant (rsID / SNP)

rs876661269

rs876661269 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GJB1. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

GJB1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xq13.1
HGVS: NM_000166.6(GJB1):c.151T>C (p.Phe51Leu)
Allele change: Silent

Associated conditions / phenotypes

Charcot-Marie-Tooth Neuropathy X

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.