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rs794728828

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728828(A;A)
Make rs794728828(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237784238
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728828
ebirs794728828
HLIrs794728828
Exacrs794728828
Varsomers794728828
Maprs794728828
PheGenIrs794728828
hapmaprs794728828
1000 genomesrs794728828
hgdprs794728828
ensemblrs794728828
gopubmedrs794728828
geneviewrs794728828
scholarrs794728828
googlers794728828
pharmgkbrs794728828
gwascentralrs794728828
openSNPrs794728828
23andMers794728828
23andMe allrs794728828
SNP Nexus

SNPshotrs794728828
SNPdbers794728828
MSV3drs794728828
GWAS Ctlgrs794728828
Max Magnitude0
ClinVar
Risk rs794728828(A;A)
Alt rs794728828(A;A)
Reference rs794728828(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947538G>A
CLNSRC
CLNACC RCV000182891.1,