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rs794728802

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728802(A;C)
Make rs794728802(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237806236
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728802
ebirs794728802
HLIrs794728802
Exacrs794728802
Varsomers794728802
Maprs794728802
PheGenIrs794728802
hapmaprs794728802
1000 genomesrs794728802
hgdprs794728802
ensemblrs794728802
gopubmedrs794728802
geneviewrs794728802
scholarrs794728802
googlers794728802
pharmgkbrs794728802
gwascentralrs794728802
openSNPrs794728802
23andMers794728802
23andMe allrs794728802
SNP Nexus

SNPshotrs794728802
SNPdbers794728802
MSV3drs794728802
GWAS Ctlgrs794728802
Max Magnitude0
ClinVar
Risk rs794728802(C;C)
Alt rs794728802(C;C)
Reference rs794728802(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237969536A>C
CLNSRC
CLNACC RCV000182843.1,