rs11224899

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common genotype

Make rs11224899(A;A)

Make rs11224899(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

97088525

is a	snp
is	mentioned by
dbSNP	rs11224899
dbSNP (classic)	rs11224899
ClinGen	rs11224899
ebi	rs11224899
HLI	rs11224899
Exac	rs11224899
Gnomad	rs11224899
Varsome	rs11224899
LitVar	rs11224899
Map	rs11224899
PheGenI	rs11224899
Biobank	rs11224899
1000 genomes	rs11224899
hgdp	rs11224899
ensembl	rs11224899
geneview	rs11224899
scholar	rs11224899
google	rs11224899
pharmgkb	rs11224899
gwascentral	rs11224899
openSNP	rs11224899
23andMe	rs11224899
SNPshot	rs11224899
SNPdbe	rs11224899
MSV3d	rs11224899
GWAS Ctlg	rs11224899

GMAF

0.09917

Max Magnitude

0

?	(A;A) (A;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	T
P-val	0.000002
Odds Ratio	1.8989 None