Variant (rsID / SNP)
rs193922886
rs193922886 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 39,074,134. Clinical significance in the table: Pathogenic.
Reference-table entries
RYR1Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:39074134
- Cytoband
- 19q13.2
- HGVS
- NM_000540.2(RYR1):c.14647-1449A>G
- Allele change
- Silent
Associated conditions / phenotypes
Congenital multicore myopathy with external ophthalmoplegia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.