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RYR2

From SNPedia

is agene
is mentioned by
Full nameryanodine receptor 2 (cardiac)
RelatedRYR1, RYR3
EntrezGene6262
PheGenI6262
VariationViewer6262
ClinVarRYR2
GeneCardsRYR2
dbSNP6262
SADR6262
HugeNav6262
wikipediaRYR2
googleRYR2
gopubmedRYR2
EVSRYR2
HEFalMpRYR2
MyGene2RYR2
23andMeRYR2
UniProtQ92736
EnsemblENSG00000198626
OMIM180902
# SNPs149
 Max MagnitudeChromosome positionSummary
rs107546020237,388,076
rs10925388237,376,053
rs1219185970237,634,937
rs1219185980237,648,523
rs1219185990237,784,024
rs1219186000237,791,441
rs1219186010237,640,938
rs1219186020237,454,396
rs1219186030237,639,068
rs1219186040237,798,037
rs1219186050237,784,314
rs1219186060237,819,181
rs1478912237,457,939
rs168352370237,423,084
rs176865730237,492,989
rs1869065980237,627,977
rs1901405980237,445,488
rs1933129237,114,311
rs1939226220237,808,916
rs1939226230237,500,774
rs1939226240237,566,603
rs1939226250237,590,872
rs1939226260237,590,901
rs2002367500237,566,672
rs2016759510237,610,770
rs20506560237,347,614
rs2056387237,760,812
rs22532730237,548,497
rs268786237,192,685
rs2819742237,826,822
rs2819770237,747,704
rs349678130237,678,090
rs3695123470237,388,129
rs3750212010237,783,759
rs37650970237,454,457
rs3975165080237,784,256
rs3975165100237,791,480
rs3975165390237,377,365
rs413158580237,614,782
rs5333306640237,550,628
rs5719857750237,785,999
rs5877829750237,772,024
rs6683225237,186,438
rs7275033960237,369,589
rs7275049760237,639,162
rs7308801870237,492,973
rs7308801910237,566,623
rs7308801960237,784,037
rs7308801990237,819,167
rs7308802000237,828,425
... further results

[PMID 24447446] Postmortem genetic screening of SNPs in RyR2 gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population.

[PMID 23651034OA-icon.png] Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population.

[PMID 23595086OA-icon.png] Genetic background of catecholaminergic polymorphic ventricular tachycardia in Japan.

[PMID 22962621OA-icon.png] Cell model of catecholaminergic polymorphic ventricular tachycardia reveals early and delayed afterdepolarizations.

[PMID 21954897] Intravenous epinephrine infusion test in diagnosis of catecholaminergic polymorphic ventricular tachycardia.

[PMID 19781797] Ryanodine receptor (RyR2) mutations in sudden cardiac death: studies in extended pedigrees and phenotypic characterization in vitro.

[PMID 19216760OA-icon.png] Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia.

[PMID 18929323] U-waves and T-wave peak to T-wave end intervals in patients with catecholaminergic polymorphic ventricular tachycardia, effects of beta-blockers.

[PMID 17347175OA-icon.png] Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves.

[PMID 15913575OA-icon.png] Catecholaminergic polymorphic ventricular tachycardia: recent mechanistic insights.

[PMID 15720454] Calcium channel antagonism reduces exercise-induced ventricular arrhythmias in catecholaminergic polymorphic ventricular tachycardia patients with RyR2 mutations.

[PMID 15271719] Volatile anesthetics and succinylcholine in cardiac ryanodine receptor defects.

[PMID 15197150OA-icon.png] Sudden death in familial polymorphic ventricular tachycardia associated with calcium release channel (ryanodine receptor) leak.

[PMID 15176428] Genes, exercise and sudden death: molecular basis of familial catecholaminergic polymorphic ventricular tachycardia.

[PMID 14571276OA-icon.png] Molecular genetics of exercise-induced polymorphic ventricular tachycardia: identification of three novel cardiac ryanodine receptor mutations and two common calsequestrin 2 amino-acid polymorphisms.

[PMID 11157710OA-icon.png] Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia.