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Variant (rsID / SNP)

rs3766871

RYR2

rs3766871 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RYR2. Location: chromosome 1, position 237,778,084. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

RYR2Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
1:237778084
Cytoband
1q43
HGVS
NM_001035.3(RYR2):c.5656G>A (p.Gly1886Ser)
Allele change
Missense_G1886S

Associated conditions / phenotypes

Cardiomyopathy|Cardiovascular phenotype|Arrhythmogenic right ventricular cardiomyopathy|Catecholaminergic polymorphic ventricular tachycardia|Catecholaminergic polymorphic ventricular tachycardia 1

Public references

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