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rs1015657

From SNPedia

Orientationminus
Stabilizedplus
Make rs1015657(C;C)
Make rs1015657(C;T)
Make rs1015657(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position70882346
is asnp
is mentioned by
dbSNPrs1015657
ebirs1015657
HLIrs1015657
Exacrs1015657
Varsomers1015657
Maprs1015657
PheGenIrs1015657
hapmaprs1015657
1000 genomesrs1015657
hgdprs1015657
ensemblrs1015657
gopubmedrs1015657
geneviewrs1015657
scholarrs1015657
googlers1015657
pharmgkbrs1015657
gwascentralrs1015657
openSNPrs1015657
23andMers1015657
23andMe allrs1015657
SNP Nexus

SNPshotrs1015657
SNPdbers1015657
MSV3drs1015657
GWAS Ctlgrs1015657
GMAF0.3659
Max Magnitude
? (C;C) (C;T) (T;T) 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
P-val 0.000002
Odds Ratio 1.3200 None