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rs863223351

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223351(A;A)
Make rs863223351(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position39218007
GeneSTAC2
is asnp
is mentioned by
dbSNPrs863223351
ebirs863223351
HLIrs863223351
Exacrs863223351
Varsomers863223351
Maprs863223351
PheGenIrs863223351
hapmaprs863223351
1000 genomesrs863223351
hgdprs863223351
ensemblrs863223351
gopubmedrs863223351
geneviewrs863223351
scholarrs863223351
googlers863223351
pharmgkbrs863223351
gwascentralrs863223351
openSNPrs863223351
23andMers863223351
23andMe allrs863223351
SNP Nexus

SNPshotrs863223351
SNPdbers863223351
MSV3drs863223351
GWAS Ctlgrs863223351
Max Magnitude0
ClinVar
Risk rs863223351(A;A)
Alt rs863223351(A;A)
Reference rs863223351(G;G)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene STAC2
CLNDBN Childhood-Onset Schizophrenia
Reversed 1
HGVS NC_000017.10:g.37374260C>T
CLNSRC
CLNACC RCV000202325.1,