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rs794728743

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728743(C;T)
Make rs794728743(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237633620
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728743
ebirs794728743
HLIrs794728743
Exacrs794728743
Varsomers794728743
Maprs794728743
PheGenIrs794728743
hapmaprs794728743
1000 genomesrs794728743
hgdprs794728743
ensemblrs794728743
gopubmedrs794728743
geneviewrs794728743
scholarrs794728743
googlers794728743
pharmgkbrs794728743
gwascentralrs794728743
openSNPrs794728743
23andMers794728743
23andMe allrs794728743
SNP Nexus

SNPshotrs794728743
SNPdbers794728743
MSV3drs794728743
GWAS Ctlgrs794728743
Max Magnitude0
ClinVar
Risk rs794728743(T;T)
Alt rs794728743(T;T)
Reference rs794728743(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237796920C>T
CLNSRC
CLNACC RCV000182744.1,