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rs4906844

From SNPedia

Orientationplus
Stabilizedplus
Make rs4906844(A;A)
Make rs4906844(A;G)
Make rs4906844(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position26032398
GeneLOC100128714
is asnp
is mentioned by
dbSNPrs4906844
dbSNP (old)rs4906844
ClinGenrs4906844
ebirs4906844
HLIrs4906844
Exacrs4906844
Gnomadrs4906844
Varsomers4906844
Maprs4906844
PheGenIrs4906844
Biobankrs4906844
1000 genomesrs4906844
hgdprs4906844
ensemblrs4906844
gopubmedrs4906844
geneviewrs4906844
scholarrs4906844
googlers4906844
pharmgkbrs4906844
gwascentralrs4906844
openSNPrs4906844
23andMers4906844
23andMe allrs4906844
SNP Nexus

SNPshotrs4906844
SNPdbers4906844
MSV3drs4906844
GWAS Ctlgrs4906844
GMAF0.377
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21810643OA-icon.png]
Trait
Title Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia.
Risk Allele
P-val 1E-8
Odds Ratio 0.0700 [NR] mm decrease