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rs794728799

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728799(C;T)
Make rs794728799(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237793906
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728799
ebirs794728799
HLIrs794728799
Exacrs794728799
Varsomers794728799
Maprs794728799
PheGenIrs794728799
hapmaprs794728799
1000 genomesrs794728799
hgdprs794728799
ensemblrs794728799
gopubmedrs794728799
geneviewrs794728799
scholarrs794728799
googlers794728799
pharmgkbrs794728799
gwascentralrs794728799
openSNPrs794728799
23andMers794728799
23andMe allrs794728799
SNP Nexus

SNPshotrs794728799
SNPdbers794728799
MSV3drs794728799
GWAS Ctlgrs794728799
Max Magnitude0
ClinVar
Risk rs794728799(T;T)
Alt rs794728799(T;T)
Reference rs794728799(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237957206C>T
CLNSRC
CLNACC RCV000182840.2,