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rs794728755

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728755(G;T)
Make rs794728755(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237640970
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728755
ebirs794728755
HLIrs794728755
Exacrs794728755
Varsomers794728755
Maprs794728755
PheGenIrs794728755
hapmaprs794728755
1000 genomesrs794728755
hgdprs794728755
ensemblrs794728755
gopubmedrs794728755
geneviewrs794728755
scholarrs794728755
googlers794728755
pharmgkbrs794728755
gwascentralrs794728755
openSNPrs794728755
23andMers794728755
23andMe allrs794728755
SNP Nexus

SNPshotrs794728755
SNPdbers794728755
MSV3drs794728755
GWAS Ctlgrs794728755
Max Magnitude0
ClinVar
Risk rs794728755(T;T)
Alt rs794728755(T;T)
Reference rs794728755(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237804270G>T
CLNSRC
CLNACC RCV000182759.2,