rs1015657

Orientation

minus

Stabilized

minus

Make rs1015657(C;C)

Make rs1015657(C;T)

Make rs1015657(T;T)

Reference

GRCh38 38.1/142

Chromosome

17

Position

70882346

is a	snp
is	mentioned by
dbSNP	rs1015657
dbSNP (classic)	rs1015657
ClinGen	rs1015657
ebi	rs1015657
HLI	rs1015657
Exac	rs1015657
Gnomad	rs1015657
Varsome	rs1015657
LitVar	rs1015657
Map	rs1015657
PheGenI	rs1015657
Biobank	rs1015657
1000 genomes	rs1015657
hgdp	rs1015657
ensembl	rs1015657
geneview	rs1015657
scholar	rs1015657
google	rs1015657
pharmgkb	rs1015657
gwascentral	rs1015657
openSNP	rs1015657
23andMe	rs1015657
SNPshot	rs1015657
SNPdbe	rs1015657
MSV3d	rs1015657
GWAS Ctlg	rs1015657

GMAF

0.3659

Max Magnitude

0

?	(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