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rs794728754

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728754(C;T)
Make rs794728754(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237640941
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728754
ebirs794728754
HLIrs794728754
Exacrs794728754
Varsomers794728754
Maprs794728754
PheGenIrs794728754
hapmaprs794728754
1000 genomesrs794728754
hgdprs794728754
ensemblrs794728754
gopubmedrs794728754
geneviewrs794728754
scholarrs794728754
googlers794728754
pharmgkbrs794728754
gwascentralrs794728754
openSNPrs794728754
23andMers794728754
23andMe allrs794728754
SNP Nexus

SNPshotrs794728754
SNPdbers794728754
MSV3drs794728754
GWAS Ctlgrs794728754
Max Magnitude0
ClinVar
Risk rs794728754(T;T)
Alt rs794728754(T;T)
Reference rs794728754(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237804241C>T
CLNSRC
CLNACC RCV000182758.1,