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rs794728810

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728810(C;C)
Make rs794728810(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237832588
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728810
ebirs794728810
HLIrs794728810
Exacrs794728810
Varsomers794728810
Maprs794728810
PheGenIrs794728810
hapmaprs794728810
1000 genomesrs794728810
hgdprs794728810
ensemblrs794728810
gopubmedrs794728810
geneviewrs794728810
scholarrs794728810
googlers794728810
pharmgkbrs794728810
gwascentralrs794728810
openSNPrs794728810
23andMers794728810
23andMe allrs794728810
SNP Nexus

SNPshotrs794728810
SNPdbers794728810
MSV3drs794728810
GWAS Ctlgrs794728810
Max Magnitude0
ClinVar
Risk rs794728810(C;C)
Alt rs794728810(C;C)
Reference rs794728810(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237995888T>C
CLNSRC
CLNACC RCV000182852.2,