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rs794728808

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728808(C;T)
Make rs794728808(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237830578
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728808
ebirs794728808
HLIrs794728808
Exacrs794728808
Varsomers794728808
Maprs794728808
PheGenIrs794728808
hapmaprs794728808
1000 genomesrs794728808
hgdprs794728808
ensemblrs794728808
gopubmedrs794728808
geneviewrs794728808
scholarrs794728808
googlers794728808
pharmgkbrs794728808
gwascentralrs794728808
openSNPrs794728808
23andMers794728808
23andMe allrs794728808
SNP Nexus

SNPshotrs794728808
SNPdbers794728808
MSV3drs794728808
GWAS Ctlgrs794728808
Max Magnitude0
ClinVar
Risk rs794728808(T;T)
Alt rs794728808(T;T)
Reference rs794728808(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237993878C>T
CLNSRC
CLNACC RCV000182850.1,