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rs794728816

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728816(A;A)
Make rs794728816(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237445424
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728816
ebirs794728816
HLIrs794728816
Exacrs794728816
Varsomers794728816
Maprs794728816
PheGenIrs794728816
hapmaprs794728816
1000 genomesrs794728816
hgdprs794728816
ensemblrs794728816
gopubmedrs794728816
geneviewrs794728816
scholarrs794728816
googlers794728816
pharmgkbrs794728816
gwascentralrs794728816
openSNPrs794728816
23andMers794728816
23andMe allrs794728816
SNP Nexus

SNPshotrs794728816
SNPdbers794728816
MSV3drs794728816
GWAS Ctlgrs794728816
Max Magnitude0
ClinVar
Risk rs794728816(A;A)
Alt rs794728816(A;A)
Reference rs794728816(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237608724C>A
CLNSRC
CLNACC RCV000182862.1,