Have questions? Visit https://www.reddit.com/r/SNPedia

rs121918604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121918604(G;T)
Make rs121918604(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position237798037
GeneRYR2
is asnp
is mentioned by
dbSNPrs121918604
ebirs121918604
HLIrs121918604
Exacrs121918604
Varsomers121918604
Maprs121918604
PheGenIrs121918604
hapmaprs121918604
1000 genomesrs121918604
hgdprs121918604
ensemblrs121918604
gopubmedrs121918604
geneviewrs121918604
scholarrs121918604
googlers121918604
pharmgkbrs121918604
gwascentralrs121918604
openSNPrs121918604
23andMers121918604
23andMe allrs121918604
SNP Nexus

SNPshotrs121918604
SNPdbers121918604
MSV3drs121918604
GWAS Ctlgrs121918604
Max Magnitude0
OMIM180902
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121918604(A,T;A,T)
Alt rs121918604(A,T;A,T)
Reference rs121918604(G;G)
Significance Other
Disease Ventricular tachycardia
Variation info
Gene RYR2
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000001.10:g.237961337G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000013827.25,