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rs794728712

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs794728712(A;A)
Make rs794728712(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237388137
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728712
ebirs794728712
HLIrs794728712
Exacrs794728712
Varsomers794728712
Maprs794728712
PheGenIrs794728712
hapmaprs794728712
1000 genomesrs794728712
hgdprs794728712
ensemblrs794728712
gopubmedrs794728712
geneviewrs794728712
scholarrs794728712
googlers794728712
pharmgkbrs794728712
gwascentralrs794728712
openSNPrs794728712
23andMers794728712
23andMe allrs794728712
SNP Nexus

SNPshotrs794728712
SNPdbers794728712
MSV3drs794728712
GWAS Ctlgrs794728712
Max Magnitude0
ClinVar
Risk rs794728712(A;A)
Alt rs794728712(A;A)
Reference rs794728712(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237551437G>A
CLNSRC
CLNACC RCV000182665.2,