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rs794728830

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728830(C;T)
Make rs794728830(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237792276
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728830
ebirs794728830
HLIrs794728830
Exacrs794728830
Varsomers794728830
Maprs794728830
PheGenIrs794728830
hapmaprs794728830
1000 genomesrs794728830
hgdprs794728830
ensemblrs794728830
gopubmedrs794728830
geneviewrs794728830
scholarrs794728830
googlers794728830
pharmgkbrs794728830
gwascentralrs794728830
openSNPrs794728830
23andMers794728830
23andMe allrs794728830
SNP Nexus

SNPshotrs794728830
SNPdbers794728830
MSV3drs794728830
GWAS Ctlgrs794728830
Max Magnitude0
ClinVar
Risk rs794728830(T;T)
Alt rs794728830(T;T)
Reference rs794728830(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237955576C>T
CLNSRC
CLNACC RCV000182893.1,