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rs121918603

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918603(C;T)
Make rs121918603(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position237639068
GeneRYR2
is asnp
is mentioned by
dbSNPrs121918603
ebirs121918603
HLIrs121918603
Exacrs121918603
Varsomers121918603
Maprs121918603
PheGenIrs121918603
hapmaprs121918603
1000 genomesrs121918603
hgdprs121918603
ensemblrs121918603
gopubmedrs121918603
geneviewrs121918603
scholarrs121918603
googlers121918603
pharmgkbrs121918603
gwascentralrs121918603
openSNPrs121918603
23andMers121918603
23andMe allrs121918603
SNP Nexus

SNPshotrs121918603
SNPdbers121918603
MSV3drs121918603
GWAS Ctlgrs121918603
Max Magnitude0
OMIM180902
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121918603(T;T)
Alt rs121918603(T;T)
Reference rs121918603(C;C)
Significance Pathogenic
Disease Ventricular tachycardia
Variation info
Gene RYR2
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000001.10:g.237802368C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013826.22,