Variant (rsID / SNP)

rs118192136

rs118192136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 39,062,824. Clinical significance in the table: Likely pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

RYR1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 19:39062824
Cytoband: 19q13.2
HGVS: NM_000540.3(RYR1):c.13912G>A (p.Gly4638Ser)
Allele change: Missense_G4633S

Associated conditions / phenotypes

Central core myopathy|RYR1-Related Disorders

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.