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rs863223350

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223350(C;T)
Make rs863223350(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position74521264
GeneGTF2IRD1
is asnp
is mentioned by
dbSNPrs863223350
ebirs863223350
HLIrs863223350
Exacrs863223350
Varsomers863223350
Maprs863223350
PheGenIrs863223350
hapmaprs863223350
1000 genomesrs863223350
hgdprs863223350
ensemblrs863223350
gopubmedrs863223350
geneviewrs863223350
scholarrs863223350
googlers863223350
pharmgkbrs863223350
gwascentralrs863223350
openSNPrs863223350
23andMers863223350
23andMe allrs863223350
SNP Nexus

SNPshotrs863223350
SNPdbers863223350
MSV3drs863223350
GWAS Ctlgrs863223350
Max Magnitude0
ClinVar
Risk rs863223350(T;T)
Alt rs863223350(T;T)
Reference rs863223350(C;C)
Significance Probable-Pathogenic
Disease Childhood-Onset Schizophrenia
Variation info
Gene GTF2IRD1
CLNDBN Childhood-Onset Schizophrenia
Reversed 0
HGVS NC_000007.13:g.73935594C>T
CLNSRC
CLNACC RCV000202332.1,