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rs794728825

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs794728825(A;C)
Make rs794728825(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237778702
GeneRYR2
is asnp
is mentioned by
dbSNPrs794728825
ebirs794728825
HLIrs794728825
Exacrs794728825
Varsomers794728825
Maprs794728825
PheGenIrs794728825
hapmaprs794728825
1000 genomesrs794728825
hgdprs794728825
ensemblrs794728825
gopubmedrs794728825
geneviewrs794728825
scholarrs794728825
googlers794728825
pharmgkbrs794728825
gwascentralrs794728825
openSNPrs794728825
23andMers794728825
23andMe allrs794728825
SNP Nexus

SNPshotrs794728825
SNPdbers794728825
MSV3drs794728825
GWAS Ctlgrs794728825
Max Magnitude0
ClinVar
Risk rs794728825(C;C)
Alt rs794728825(C;C)
Reference rs794728825(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RYR2
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.237942002A>C
CLNSRC
CLNACC RCV000182886.1,