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rs10263087

From SNPedia

Orientationplus
Stabilizedplus
Make rs10263087(C;C)
Make rs10263087(C;G)
Make rs10263087(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position155178759
is asnp
is mentioned by
dbSNPrs10263087
ebirs10263087
HLIrs10263087
Exacrs10263087
Varsomers10263087
Maprs10263087
PheGenIrs10263087
hapmaprs10263087
1000 genomesrs10263087
hgdprs10263087
ensemblrs10263087
gopubmedrs10263087
geneviewrs10263087
scholarrs10263087
googlers10263087
pharmgkbrs10263087
gwascentralrs10263087
openSNPrs10263087
23andMers10263087
23andMe allrs10263087
SNP Nexus

SNPshotrs10263087
SNPdbers10263087
MSV3drs10263087
GWAS Ctlgrs10263087
GMAF0.1777
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22648509]
Trait
Title PKNOX2 is Associated with Formal Thought Disorder in Schizophrenia: a Meta-Analysis of Two Genome-wide Association Studies.
Risk Allele C
P-val 0.000007
Odds Ratio 1.5470 None