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rs794728704

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs794728704(A;A)
Make rs794728704(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237778704
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728704
ebirs794728704
HLIrs794728704
Exacrs794728704
Varsomers794728704
Maprs794728704
PheGenIrs794728704
hapmaprs794728704
1000 genomesrs794728704
hgdprs794728704
ensemblrs794728704
gopubmedrs794728704
geneviewrs794728704
scholarrs794728704
googlers794728704
pharmgkbrs794728704
gwascentralrs794728704
openSNPrs794728704
23andMers794728704
23andMe allrs794728704
SNP Nexus

SNPshotrs794728704
SNPdbers794728704
MSV3drs794728704
GWAS Ctlgrs794728704
Max Magnitude0
ClinVar
Risk rs794728704(A;A)
Alt rs794728704(A;A)
Reference rs794728704(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237942004C>A
CLNSRC
CLNACC RCV000182651.1,