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rs794728832

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728832(A;G)
Make rs794728832(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237832628
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728832
ebirs794728832
HLIrs794728832
Exacrs794728832
Varsomers794728832
Maprs794728832
PheGenIrs794728832
hapmaprs794728832
1000 genomesrs794728832
hgdprs794728832
ensemblrs794728832
gopubmedrs794728832
geneviewrs794728832
scholarrs794728832
googlers794728832
pharmgkbrs794728832
gwascentralrs794728832
openSNPrs794728832
23andMers794728832
23andMe allrs794728832
SNP Nexus

SNPshotrs794728832
SNPdbers794728832
MSV3drs794728832
GWAS Ctlgrs794728832
Max Magnitude0
ClinVar
Risk rs794728832(G;G)
Alt rs794728832(G;G)
Reference rs794728832(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237995928A>G
CLNSRC
CLNACC RCV000182895.1,