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rs878854365

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854365(C;T)
Make rs878854365(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position38458154
GeneRYR1
is asnp
is mentioned by
dbSNPrs878854365
ebirs878854365
HLIrs878854365
Exacrs878854365
Varsomers878854365
Maprs878854365
PheGenIrs878854365
hapmaprs878854365
1000 genomesrs878854365
hgdprs878854365
ensemblrs878854365
gopubmedrs878854365
geneviewrs878854365
scholarrs878854365
googlers878854365
pharmgkbrs878854365
gwascentralrs878854365
openSNPrs878854365
23andMers878854365
23andMe allrs878854365
SNP Nexus

SNPshotrs878854365
SNPdbers878854365
MSV3drs878854365
GWAS Ctlgrs878854365
Max Magnitude0
ClinVar
Risk rs878854365(T;T)
Alt rs878854365(T;T)
Reference rs878854365(C;C)
Significance Probable-Pathogenic
Disease Central core disease
Variation info
Gene RYR1
CLNDBN Central core disease
Reversed 0
HGVS NC_000019.9:g.38948794C>T
CLNSRC
CLNACC RCV000226744.1,