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rs10744743

From SNPedia

Orientationplus
Stabilizedplus
Make rs10744743(C;C)
Make rs10744743(C;G)
Make rs10744743(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position119805261
GeneCIT
is asnp
is mentioned by
dbSNPrs10744743
ebirs10744743
HLIrs10744743
Exacrs10744743
Varsomers10744743
Maprs10744743
PheGenIrs10744743
hapmaprs10744743
1000 genomesrs10744743
hgdprs10744743
ensemblrs10744743
gopubmedrs10744743
geneviewrs10744743
scholarrs10744743
googlers10744743
pharmgkbrs10744743
gwascentralrs10744743
openSNPrs10744743
23andMers10744743
23andMe allrs10744743
SNP Nexus

SNPshotrs10744743
SNPdbers10744743
MSV3drs10744743
GWAS Ctlgrs10744743
GMAF0.3636
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 20084519] Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging