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rs11038167

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11038167(A;C)
Make rs11038167(C;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position44821583
GeneTSPAN18
is asnp
is mentioned by
dbSNPrs11038167
ebirs11038167
HLIrs11038167
Exacrs11038167
Varsomers11038167
Maprs11038167
PheGenIrs11038167
hapmaprs11038167
1000 genomesrs11038167
hgdprs11038167
ensemblrs11038167
gopubmedrs11038167
geneviewrs11038167
scholarrs11038167
googlers11038167
pharmgkbrs11038167
gwascentralrs11038167
openSNPrs11038167
23andMers11038167
23andMe allrs11038167
SNP Nexus

SNPshotrs11038167
SNPdbers11038167
MSV3drs11038167
GWAS Ctlgrs11038167
GMAF0.1901
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 22037552]
Trait
Title Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2.
Risk Allele
P-val 1E-11
Odds Ratio 1.2900 None


[PMID 23505562OA-icon.png] Replication Study Confirms Link between TSPAN18 Mutation and Schizophrenia in Han Chinese