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rs4798896

From SNPedia

Orientationplus
Stabilizedplus
Make rs4798896(A;A)
Make rs4798896(A;G)
Make rs4798896(G;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position78152922
is asnp
is mentioned by
dbSNPrs4798896
ebirs4798896
HLIrs4798896
Exacrs4798896
Varsomers4798896
Maprs4798896
PheGenIrs4798896
hapmaprs4798896
1000 genomesrs4798896
hgdprs4798896
ensemblrs4798896
gopubmedrs4798896
geneviewrs4798896
scholarrs4798896
googlers4798896
pharmgkbrs4798896
gwascentralrs4798896
openSNPrs4798896
23andMers4798896
23andMe allrs4798896
SNP Nexus

SNPshotrs4798896
SNPdbers4798896
MSV3drs4798896
GWAS Ctlgrs4798896
GMAF0.3627
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23212062OA-icon.png]
Trait Schizophrenia
Title Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
Risk Allele
P-val 4E-6
Odds Ratio .09 [NR] unit increase