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rs1391768

From SNPedia

Orientationminus
Stabilizedminus
Make rs1391768(C;C)
Make rs1391768(C;T)
Make rs1391768(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position8437548
GeneNDEL1
is asnp
is mentioned by
dbSNPrs1391768
ebirs1391768
HLIrs1391768
Exacrs1391768
Varsomers1391768
Maprs1391768
PheGenIrs1391768
hapmaprs1391768
1000 genomesrs1391768
hgdprs1391768
ensemblrs1391768
gopubmedrs1391768
geneviewrs1391768
scholarrs1391768
googlers1391768
pharmgkbrs1391768
gwascentralrs1391768
openSNPrs1391768
23andMers1391768
23andMe allrs1391768
SNP Nexus

SNPshotrs1391768
SNPdbers1391768
MSV3drs1391768
GWAS Ctlgrs1391768
GMAF0.4109
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 18469341OA-icon.png] 275 Caucasian schizophrenia patients and 200 controls rs1391768 imparting a significant effect but only in the context of a Cys carrying background


[PMID 19251251OA-icon.png] Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.