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rs863223355

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863223355(A;C)
Make rs863223355(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237500745
GeneRYR2
is asnp
is mentioned by
dbSNPrs863223355
ebirs863223355
HLIrs863223355
Exacrs863223355
Varsomers863223355
Maprs863223355
PheGenIrs863223355
hapmaprs863223355
1000 genomesrs863223355
hgdprs863223355
ensemblrs863223355
gopubmedrs863223355
geneviewrs863223355
scholarrs863223355
googlers863223355
pharmgkbrs863223355
gwascentralrs863223355
openSNPrs863223355
23andMers863223355
23andMe allrs863223355
SNP Nexus

SNPshotrs863223355
SNPdbers863223355
MSV3drs863223355
GWAS Ctlgrs863223355
Max Magnitude0
ClinVar
Risk rs863223355(C;C)
Alt rs863223355(C;C)
Reference rs863223355(A;A)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene RYR2
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000001.10:g.237664045A>C
CLNSRC
CLNACC RCV000202329.1,