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rs193922626

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922626(C;C)
Make rs193922626(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position237590901
GeneRYR2
is asnp
is mentioned by
dbSNPrs193922626
ebirs193922626
HLIrs193922626
Exacrs193922626
Varsomers193922626
Maprs193922626
PheGenIrs193922626
hapmaprs193922626
1000 genomesrs193922626
hgdprs193922626
ensemblrs193922626
gopubmedrs193922626
geneviewrs193922626
scholarrs193922626
googlers193922626
pharmgkbrs193922626
gwascentralrs193922626
openSNPrs193922626
23andMers193922626
23andMe allrs193922626
SNP Nexus

SNPshotrs193922626
SNPdbers193922626
MSV3drs193922626
GWAS Ctlgrs193922626
Max Magnitude0
ClinVar
Risk rs193922626(A,C;A,C)
Alt rs193922626(A,C;A,C)
Reference rs193922626(G;G)
Significance Probable-Pathogenic
Disease Cardiomyopathy not specified
Variation info
Gene RYR2
CLNDBN Cardiomyopathy not specified
Reversed 0
HGVS NC_000001.10:g.237754201G>C
CLNSRC ClinVar LabCorp
CLNACC RCV000030422.1, RCV000154818.1,