Variant (rsID / SNP)
rs55806270
rs55806270 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHRNE. Location: chromosome 17, position 4,802,025. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
CHRNEBenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:4802025
- Cytoband
- 17p13.2
- HGVS
- NM_000080.4(CHRNE):c.*6A>G
- Allele change
- Silent
Associated conditions / phenotypes
Congenital myasthenic syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.