Variant (rsID / SNP)
rs193922878
rs193922878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 39,071,010. Clinical significance in the table: Likely pathogenic; drug response.
Reference-table entries
RYR1Likely pathogenic
- Clinical significance (as recorded)
- Likely pathogenic; drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:39071010
- Cytoband
- 19q13.2
- HGVS
- NM_000540.3(RYR1):c.14512C>G (p.Leu4838Val)
- Allele change
- Missense_L4833V
Associated conditions / phenotypes
enflurane response - Toxicity|desflurane response - Toxicity|halothane response - Toxicity|isoflurane response - Toxicity|methoxyflurane response - Toxicity|sevoflurane response - Toxicity|succinylcholine response - Toxicity|Malignant hyperthermia, susceptibility to, 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.