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rs794728798

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728798(C;C)
Make rs794728798(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237791472
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728798
ebirs794728798
HLIrs794728798
Exacrs794728798
Varsomers794728798
Maprs794728798
PheGenIrs794728798
hapmaprs794728798
1000 genomesrs794728798
hgdprs794728798
ensemblrs794728798
gopubmedrs794728798
geneviewrs794728798
scholarrs794728798
googlers794728798
pharmgkbrs794728798
gwascentralrs794728798
openSNPrs794728798
23andMers794728798
23andMe allrs794728798
SNP Nexus

SNPshotrs794728798
SNPdbers794728798
MSV3drs794728798
GWAS Ctlgrs794728798
Max Magnitude0
ClinVar
Risk rs794728798(C;C)
Alt rs794728798(C;C)
Reference rs794728798(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene RYR2
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.237954772T>C
CLNSRC
CLNACC RCV000223697.1,