Variant (rsID / SNP)

rs756138074

rs756138074 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR1. Location: chromosome 19, position 38,958,433. 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: 19:38958433
Cytoband: 19q13.2
HGVS: NM_000540.3(RYR1):c.3362A>G (p.Tyr1121Cys)
Allele change: Missense_Y1121C

Associated conditions / phenotypes

Inborn genetic diseases|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.