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rs794728782

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728782(C;T)
Make rs794728782(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237783980
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728782
ebirs794728782
HLIrs794728782
Exacrs794728782
Varsomers794728782
Maprs794728782
PheGenIrs794728782
hapmaprs794728782
1000 genomesrs794728782
hgdprs794728782
ensemblrs794728782
gopubmedrs794728782
geneviewrs794728782
scholarrs794728782
googlers794728782
pharmgkbrs794728782
gwascentralrs794728782
openSNPrs794728782
23andMers794728782
23andMe allrs794728782
SNP Nexus

SNPshotrs794728782
SNPdbers794728782
MSV3drs794728782
GWAS Ctlgrs794728782
Max Magnitude0
ClinVar
Risk rs794728782(T;T)
Alt rs794728782(T;T)
Reference rs794728782(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947280C>T
CLNSRC
CLNACC RCV000182810.1,