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

rs794728780

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728780(A;G)
Make rs794728780(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237783707
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728780
ebirs794728780
HLIrs794728780
Exacrs794728780
Varsomers794728780
Maprs794728780
PheGenIrs794728780
hapmaprs794728780
1000 genomesrs794728780
hgdprs794728780
ensemblrs794728780
gopubmedrs794728780
geneviewrs794728780
scholarrs794728780
googlers794728780
pharmgkbrs794728780
gwascentralrs794728780
openSNPrs794728780
23andMers794728780
23andMe allrs794728780
SNP Nexus

SNPshotrs794728780
SNPdbers794728780
MSV3drs794728780
GWAS Ctlgrs794728780
Max Magnitude0
ClinVar
Risk rs794728780(G,T;G,T)
Alt rs794728780(G,T;G,T)
Reference rs794728780(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237947007A>G; NC_000001.10:g.237947007A>T
CLNSRC
CLNACC RCV000182805.1, RCV000182890.2,