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rs794728805

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728805(A;A)
Make rs794728805(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237819067
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728805
ebirs794728805
HLIrs794728805
Exacrs794728805
Varsomers794728805
Maprs794728805
PheGenIrs794728805
hapmaprs794728805
1000 genomesrs794728805
hgdprs794728805
ensemblrs794728805
gopubmedrs794728805
geneviewrs794728805
scholarrs794728805
googlers794728805
pharmgkbrs794728805
gwascentralrs794728805
openSNPrs794728805
23andMers794728805
23andMe allrs794728805
SNP Nexus

SNPshotrs794728805
SNPdbers794728805
MSV3drs794728805
GWAS Ctlgrs794728805
Max Magnitude0
ClinVar
Risk rs794728805(A;A)
Alt rs794728805(A;A)
Reference rs794728805(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237982367G>A
CLNSRC
CLNACC RCV000182847.1,