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rs193922623

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922623(A;A)
Make rs193922623(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position237500774
GeneRYR2
is asnp
is mentioned by
dbSNPrs193922623
ebirs193922623
HLIrs193922623
Exacrs193922623
Varsomers193922623
Maprs193922623
PheGenIrs193922623
hapmaprs193922623
1000 genomesrs193922623
hgdprs193922623
ensemblrs193922623
gopubmedrs193922623
geneviewrs193922623
scholarrs193922623
googlers193922623
pharmgkbrs193922623
gwascentralrs193922623
openSNPrs193922623
23andMers193922623
23andMe allrs193922623
SNP Nexus

SNPshotrs193922623
SNPdbers193922623
MSV3drs193922623
GWAS Ctlgrs193922623
Max Magnitude0
ClinVar
Risk rs193922623(A;A)
Alt rs193922623(A;A)
Reference rs193922623(G;G)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia not specified VENTRICULAR FIBRILLATION
Variation info
Gene RYR2
CLNDBN Cardiac arrhythmia not specified VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL
Reversed 0
HGVS NC_000001.10:g.237664074G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030418.1, RCV000036714.4, RCV000157446.1,