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rs794728749

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728749(A;A)
Make rs794728749(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237639035
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728749
ebirs794728749
HLIrs794728749
Exacrs794728749
Varsomers794728749
Maprs794728749
PheGenIrs794728749
hapmaprs794728749
1000 genomesrs794728749
hgdprs794728749
ensemblrs794728749
gopubmedrs794728749
geneviewrs794728749
scholarrs794728749
googlers794728749
pharmgkbrs794728749
gwascentralrs794728749
openSNPrs794728749
23andMers794728749
23andMe allrs794728749
SNP Nexus

SNPshotrs794728749
SNPdbers794728749
MSV3drs794728749
GWAS Ctlgrs794728749
Max Magnitude0
ClinVar
Risk rs794728749(A;A)
Alt rs794728749(A;A)
Reference rs794728749(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237802335G>A
CLNSRC
CLNACC RCV000182751.1,