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rs863223356

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223356(C;C)
Make rs863223356(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position65661693
GeneLOC105369347, RELA
is asnp
is mentioned by
dbSNPrs863223356
ebirs863223356
HLIrs863223356
Exacrs863223356
Varsomers863223356
Maprs863223356
PheGenIrs863223356
hapmaprs863223356
1000 genomesrs863223356
hgdprs863223356
ensemblrs863223356
gopubmedrs863223356
geneviewrs863223356
scholarrs863223356
googlers863223356
pharmgkbrs863223356
gwascentralrs863223356
openSNPrs863223356
23andMers863223356
23andMe allrs863223356
SNP Nexus

SNPshotrs863223356
SNPdbers863223356
MSV3drs863223356
GWAS Ctlgrs863223356
Max Magnitude0
ClinVar
Risk rs863223356(C;C)
Alt rs863223356(C;C)
Reference rs863223356(T;T)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene RELA
CLNDBN Childhood-Onset Schizophrenia
Reversed 1
HGVS NC_000011.9:g.65429164A>G
CLNSRC
CLNACC RCV000202330.1,