Variant (rsID / SNP)

rs772494345

rs772494345 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 39,051,969. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

RYR1Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 19:39051969
Cytoband: 19q13.2
HGVS: NM_000540.3(RYR1):c.12499G>T (p.Glu4167Ter)
Allele change: Nonsense_E4162X

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.