Variant (rsID / SNP)
rs118192161
rs118192161 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 38,934,851. Clinical significance in the table: Pathogenic; drug response.
Reference-table entries
RYR1Pathogenic
- Clinical significance (as recorded)
- Pathogenic; drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:38934851
- Cytoband
- 19q13.2
- HGVS
- NM_000540.3(RYR1):c.487C>T (p.Arg163Cys)
- Allele change
- Missense_R163C
Associated conditions / phenotypes
Malignant hyperthermia, susceptibility to, 1|Central core myopathy|RYR1-Related Disorders|sevoflurane response - Toxicity|succinylcholine response - Toxicity|enflurane response - Toxicity|isoflurane response - Toxicity|desflurane response - Toxicity|halothane response - Toxicity|methoxyflurane response - Toxicity
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.