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rs193922622

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs193922622(A;A)
Make rs193922622(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position237808916
GeneRYR2
is asnp
is mentioned by
dbSNPrs193922622
ebirs193922622
HLIrs193922622
Exacrs193922622
Varsomers193922622
Maprs193922622
PheGenIrs193922622
hapmaprs193922622
1000 genomesrs193922622
hgdprs193922622
ensemblrs193922622
gopubmedrs193922622
geneviewrs193922622
scholarrs193922622
googlers193922622
pharmgkbrs193922622
gwascentralrs193922622
openSNPrs193922622
23andMers193922622
23andMe allrs193922622
SNP Nexus

SNPshotrs193922622
SNPdbers193922622
MSV3drs193922622
GWAS Ctlgrs193922622
Max Magnitude0
ClinVar
Risk rs193922622(A;A)
Alt rs193922622(A;A)
Reference rs193922622(G;G)
Significance Probable-Pathogenic
Disease Cardiac arrhythmia not provided
Variation info
Gene RYR2
CLNDBN Cardiac arrhythmia not provided
Reversed 0
HGVS NC_000001.10:g.237972216G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030413.1, RCV000182846.1,