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rs794728720

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728720(G;T)
Make rs794728720(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237445450
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728720
ebirs794728720
HLIrs794728720
Exacrs794728720
Varsomers794728720
Maprs794728720
PheGenIrs794728720
hapmaprs794728720
1000 genomesrs794728720
hgdprs794728720
ensemblrs794728720
gopubmedrs794728720
geneviewrs794728720
scholarrs794728720
googlers794728720
pharmgkbrs794728720
gwascentralrs794728720
openSNPrs794728720
23andMers794728720
23andMe allrs794728720
SNP Nexus

SNPshotrs794728720
SNPdbers794728720
MSV3drs794728720
GWAS Ctlgrs794728720
Max Magnitude0
ClinVar
Risk rs794728720(T;T)
Alt rs794728720(T;T)
Reference rs794728720(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237608750G>T
CLNSRC
CLNACC RCV000182677.1,