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rs794728827

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794728827(A;A)
Make rs794728827(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237781638
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728827
ebirs794728827
HLIrs794728827
Exacrs794728827
Varsomers794728827
Maprs794728827
PheGenIrs794728827
hapmaprs794728827
1000 genomesrs794728827
hgdprs794728827
ensemblrs794728827
gopubmedrs794728827
geneviewrs794728827
scholarrs794728827
googlers794728827
pharmgkbrs794728827
gwascentralrs794728827
openSNPrs794728827
23andMers794728827
23andMe allrs794728827
SNP Nexus

SNPshotrs794728827
SNPdbers794728827
MSV3drs794728827
GWAS Ctlgrs794728827
Max Magnitude0
ClinVar
Risk rs794728827(A;A)
Alt rs794728827(A;A)
Reference rs794728827(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237944938T>A
CLNSRC
CLNACC RCV000182889.1,