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rs10489202

From SNPedia

Orientationplus
Stabilizedplus
Make rs10489202(G;G)
Make rs10489202(G;T)
Make rs10489202(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position167933841
GeneBRP44
is asnp
is mentioned by
dbSNPrs10489202
ebirs10489202
HLIrs10489202
Exacrs10489202
Varsomers10489202
Maprs10489202
PheGenIrs10489202
hapmaprs10489202
1000 genomesrs10489202
hgdprs10489202
ensemblrs10489202
gopubmedrs10489202
geneviewrs10489202
scholarrs10489202
googlers10489202
pharmgkbrs10489202
gwascentralrs10489202
openSNPrs10489202
23andMers10489202
23andMe allrs10489202
SNP Nexus

SNPshotrs10489202
SNPdbers10489202
MSV3drs10489202
GWAS Ctlgrs10489202
GMAF0.1772
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 22037555OA-icon.png]
Trait
Title Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.
Risk Allele A
P-val 1E-8
Odds Ratio 1.2300 None


[PMID 23933155] Lack of association between MPC2 variants and schizophrenia in a replication study of Han Chinese