Have questions? Visit https://www.reddit.com/r/SNPedia

rs794728779

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728779(A;C)
Make rs794728779(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237783677
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728779
ebirs794728779
HLIrs794728779
Exacrs794728779
Varsomers794728779
Maprs794728779
PheGenIrs794728779
hapmaprs794728779
1000 genomesrs794728779
hgdprs794728779
ensemblrs794728779
gopubmedrs794728779
geneviewrs794728779
scholarrs794728779
googlers794728779
pharmgkbrs794728779
gwascentralrs794728779
openSNPrs794728779
23andMers794728779
23andMe allrs794728779
SNP Nexus

SNPshotrs794728779
SNPdbers794728779
MSV3drs794728779
GWAS Ctlgrs794728779
Max Magnitude0
ClinVar
Risk rs794728779(C,G;C,G)
Alt rs794728779(C,G;C,G)
Reference rs794728779(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237946977A>C; NC_000001.10:g.237946977A>G
CLNSRC
CLNACC RCV000182803.2, RCV000182804.1,