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rs762237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs762237(C;T)
Make rs762237(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position33035869
is asnp
is mentioned by
dbSNPrs762237
ebirs762237
HLIrs762237
Exacrs762237
Varsomers762237
Maprs762237
PheGenIrs762237
hapmaprs762237
1000 genomesrs762237
hgdprs762237
ensemblrs762237
gopubmedrs762237
geneviewrs762237
scholarrs762237
googlers762237
pharmgkbrs762237
gwascentralrs762237
openSNPrs762237
23andMers762237
23andMe allrs762237
SNP Nexus

SNPshotrs762237
SNPdbers762237
MSV3drs762237
GWAS Ctlgrs762237
GMAF0.2337
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 19477230] Evidence that variation in the oligodendrocyte lineage transcription factor 2 (OLIG2) gene is associated with psychosis in Alzheimer's disease


[PMID 16891421OA-icon.png] Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia.