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rs863223354

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223354(C;T)
Make rs863223354(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position237500743
GeneRYR2
is asnp
is mentioned by
dbSNPrs863223354
ebirs863223354
HLIrs863223354
Exacrs863223354
Varsomers863223354
Maprs863223354
PheGenIrs863223354
hapmaprs863223354
1000 genomesrs863223354
hgdprs863223354
ensemblrs863223354
gopubmedrs863223354
geneviewrs863223354
scholarrs863223354
googlers863223354
pharmgkbrs863223354
gwascentralrs863223354
openSNPrs863223354
23andMers863223354
23andMe allrs863223354
SNP Nexus

SNPshotrs863223354
SNPdbers863223354
MSV3drs863223354
GWAS Ctlgrs863223354
Max Magnitude0
ClinVar
Risk rs863223354(T;T)
Alt rs863223354(T;T)
Reference rs863223354(C;C)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene RYR2
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000001.10:g.237664043C>T
CLNSRC
CLNACC RCV000202345.1,