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rs10789369

From SNPedia

Orientationplus
Stabilizedplus
Make rs10789369(A;A)
Make rs10789369(A;G)
Make rs10789369(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position73359226
is asnp
is mentioned by
dbSNPrs10789369
ebirs10789369
HLIrs10789369
Exacrs10789369
Varsomers10789369
Maprs10789369
PheGenIrs10789369
hapmaprs10789369
1000 genomesrs10789369
hgdprs10789369
ensemblrs10789369
gopubmedrs10789369
geneviewrs10789369
scholarrs10789369
googlers10789369
pharmgkbrs10789369
gwascentralrs10789369
openSNPrs10789369
23andMers10789369
23andMe allrs10789369
SNP Nexus

SNPshotrs10789369
SNPdbers10789369
MSV3drs10789369
GWAS Ctlgrs10789369
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23974872OA-icon.png]
Trait Schizophrenia
Title Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Risk Allele A
P-val 4E-10
Odds Ratio 1.10 [1.07-1.12]