Variant (rsID / SNP)

rs201211033

rs201211033 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR2. Location: chromosome 1, position 237,540,715. Clinical significance in the table: Uncertain significance.

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Reference-table entries

RYR2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:237540715
Cytoband: 1q43
HGVS: NM_001035.3(RYR2):c.556G>A (p.Val186Met)
Allele change: Missense_V186M

Associated conditions / phenotypes

Polymorphic ventricular tachycardia|Catecholaminergic polymorphic ventricular tachycardia|Cardiomyopathy

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.