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Variant (rsID / SNP)

rs774666035

RYR1

rs774666035 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 39,006,717. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

RYR1Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
19:39006717
Cytoband
19q13.2
HGVS
NM_000540.3(RYR1):c.9555-10C>T
Allele change
Silent

Associated conditions / phenotypes

Central core myopathy|Multiminicore myopathy|Malignant hyperthermia of anesthesia|Neuromuscular disease, congenital, with uniform type 1 fiber|RYR1-Related Disorders

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.