Have questions? Visit https://www.reddit.com/r/SNPedia

rs4729938

From SNPedia

Orientationplus
Stabilizedplus
Make rs4729938(C;C)
Make rs4729938(C;G)
Make rs4729938(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position78008062
is asnp
is mentioned by
dbSNPrs4729938
ebirs4729938
HLIrs4729938
Exacrs4729938
Varsomers4729938
Maprs4729938
PheGenIrs4729938
hapmaprs4729938
1000 genomesrs4729938
hgdprs4729938
ensemblrs4729938
gopubmedrs4729938
geneviewrs4729938
scholarrs4729938
googlers4729938
pharmgkbrs4729938
gwascentralrs4729938
openSNPrs4729938
23andMers4729938
23andMe allrs4729938
SNP Nexus

SNPshotrs4729938
SNPdbers4729938
MSV3drs4729938
GWAS Ctlgrs4729938
GMAF0.3471
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