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rs11699237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C)
Make rs11699237(C;T)
Make rs11699237(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position57108940
is asnp
is mentioned by
dbSNPrs11699237
ebirs11699237
HLIrs11699237
Exacrs11699237
Varsomers11699237
Maprs11699237
PheGenIrs11699237
hapmaprs11699237
1000 genomesrs11699237
hgdprs11699237
ensemblrs11699237
gopubmedrs11699237
geneviewrs11699237
scholarrs11699237
googlers11699237
pharmgkbrs11699237
gwascentralrs11699237
openSNPrs11699237
23andMers11699237
23andMe allrs11699237
SNP Nexus

SNPshotrs11699237
SNPdbers11699237
MSV3drs11699237
GWAS Ctlgrs11699237
GMAF0.09183
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23212062OA-icon.png]
Trait Schizophrenia
Title Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
Risk Allele
P-val 3E-6
Odds Ratio .12 [NR] unit increase