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rs863223348

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223348(C;T)
Make rs863223348(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position89523356
GeneGALNT4, POC1B, POC1B-GALNT4
is asnp
is mentioned by
dbSNPrs863223348
ebirs863223348
HLIrs863223348
Exacrs863223348
Varsomers863223348
Maprs863223348
PheGenIrs863223348
hapmaprs863223348
1000 genomesrs863223348
hgdprs863223348
ensemblrs863223348
gopubmedrs863223348
geneviewrs863223348
scholarrs863223348
googlers863223348
pharmgkbrs863223348
gwascentralrs863223348
openSNPrs863223348
23andMers863223348
23andMe allrs863223348
SNP Nexus

SNPshotrs863223348
SNPdbers863223348
MSV3drs863223348
GWAS Ctlgrs863223348
Max Magnitude0
ClinVar
Risk rs863223348(T;T)
Alt rs863223348(T;T)
Reference rs863223348(C;C)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene POC1B-GALNT4 POC1B GALNT4
CLNDBN Childhood-Onset Schizophrenia
Reversed 1
HGVS NC_000012.11:g.89917133G>A
CLNSRC
CLNACC RCV000202342.1,