Variant (rsID / SNP)
rs80356692
rs80356692 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLCN1. Location: chromosome 7, position 143,027,948. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
CLCN1Pathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:143027948
- Cytoband
- 7q34
- HGVS
- NM_000083.3(CLCN1):c.937G>A (p.Ala313Thr)
- Allele change
- Missense_A313T
Associated conditions / phenotypes
Congenital myotonia, autosomal dominant form|Congenital myotonia, autosomal recessive form|Congenital myotonia, autosomal recessive form
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.