Variant (rsID / SNP)
rs6962852
rs6962852 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CLCN1. Location: chromosome 7, position 143,016,928. Clinical significance in the table: Benign.
Reference-table entries
CLCN1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:143016928
- Cytoband
- 7q34
- HGVS
- NM_000083.3(CLCN1):c.261C>T (p.Thr87=)
- Allele change
- Synonymous_T87T
Associated conditions / phenotypes
Batten-Turner congenital myopathy|Congenital myotonia, autosomal dominant form|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.