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rs730880201

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880201(C;T)
Make rs730880201(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237830600
GeneRYR2
is asnp
is mentioned by
dbSNPrs730880201
ebirs730880201
HLIrs730880201
Exacrs730880201
Varsomers730880201
Maprs730880201
PheGenIrs730880201
hapmaprs730880201
1000 genomesrs730880201
hgdprs730880201
ensemblrs730880201
gopubmedrs730880201
geneviewrs730880201
scholarrs730880201
googlers730880201
pharmgkbrs730880201
gwascentralrs730880201
openSNPrs730880201
23andMers730880201
23andMe allrs730880201
SNP Nexus

SNPshotrs730880201
SNPdbers730880201
MSV3drs730880201
GWAS Ctlgrs730880201
Max Magnitude0
ClinVar
Risk rs730880201(T;T)
Alt rs730880201(T;T)
Reference rs730880201(C;C)
Significance Probable-Pathogenic
Disease Ventricular tachycardia
Variation info
Gene RYR2
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000001.10:g.237993900C>T
CLNSRC
CLNACC RCV000157470.1,