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rs193922625

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs193922625(G;G)
Make rs193922625(G;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position237590872
GeneRYR2
is asnp
is mentioned by
dbSNPrs193922625
ebirs193922625
HLIrs193922625
Exacrs193922625
Varsomers193922625
Maprs193922625
PheGenIrs193922625
hapmaprs193922625
1000 genomesrs193922625
hgdprs193922625
ensemblrs193922625
gopubmedrs193922625
geneviewrs193922625
scholarrs193922625
googlers193922625
pharmgkbrs193922625
gwascentralrs193922625
openSNPrs193922625
23andMers193922625
23andMe allrs193922625
SNP Nexus

SNPshotrs193922625
SNPdbers193922625
MSV3drs193922625
GWAS Ctlgrs193922625
Max Magnitude0
ClinVar
Risk rs193922625(G;G)
Alt rs193922625(G;G)
Reference rs193922625(T;T)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia not specified
Variation info
Gene RYR2
CLNDBN Cardiac arrhythmia not specified
Reversed 0
HGVS NC_000001.10:g.237754172T>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030421.1, RCV000223835.1,