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rs2190665

From SNPedia

Orientationplus
Stabilizedplus
Make rs2190665(C;C)
Make rs2190665(C;G)
Make rs2190665(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position78692843
GeneMAGI2
is asnp
is mentioned by
dbSNPrs2190665
ebirs2190665
HLIrs2190665
Exacrs2190665
Varsomers2190665
Maprs2190665
PheGenIrs2190665
hapmaprs2190665
1000 genomesrs2190665
hgdprs2190665
ensemblrs2190665
gopubmedrs2190665
geneviewrs2190665
scholarrs2190665
googlers2190665
pharmgkbrs2190665
gwascentralrs2190665
openSNPrs2190665
23andMers2190665
23andMe allrs2190665
SNP Nexus

SNPshotrs2190665
SNPdbers2190665
MSV3drs2190665
GWAS Ctlgrs2190665
GMAF0.478
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 22649501OA-icon.png] Common Variants in MAGI2 Gene Are Associated with Increased Risk for Cognitive Impairment in Schizophrenic Patients