Variant (rsID / SNP)

rs118192158

rs118192158 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 39,076,592. Clinical significance in the table: Uncertain significance.

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Reference-table entries

RYR1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 19:39076592
Cytoband: 19q13.2
HGVS: NM_000540.3(RYR1):c.14818G>A (p.Ala4940Thr)
Allele change: Missense_A4935T

Associated conditions / phenotypes

Central core myopathy|RYR1-Related Disorders|Malignant hyperthermia, susceptibility to, 1|Myopathy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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