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rs730880196

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880196(A;G)
Make rs730880196(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position237784037
GeneRYR2
is asnp
is mentioned by
dbSNPrs730880196
ebirs730880196
HLIrs730880196
Exacrs730880196
Varsomers730880196
Maprs730880196
PheGenIrs730880196
hapmaprs730880196
1000 genomesrs730880196
hgdprs730880196
ensemblrs730880196
gopubmedrs730880196
geneviewrs730880196
scholarrs730880196
googlers730880196
pharmgkbrs730880196
gwascentralrs730880196
openSNPrs730880196
23andMers730880196
23andMe allrs730880196
SNP Nexus

SNPshotrs730880196
SNPdbers730880196
MSV3drs730880196
GWAS Ctlgrs730880196
Max Magnitude0
ClinVar
Risk rs730880196(G;G)
Alt rs730880196(G;G)
Reference rs730880196(A;A)
Significance Probable-Pathogenic
Disease Ventricular tachycardia
Variation info
Gene RYR2
CLNDBN Ventricular tachycardia, catecholaminergic polymorphic, 1
Reversed 0
HGVS NC_000001.10:g.237947337A>G
CLNSRC
CLNACC RCV000157465.1,