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rs17597926

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17597926(A;A)
Make rs17597926(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position55538707
GeneTCF4
is asnp
is mentioned by
dbSNPrs17597926
ebirs17597926
HLIrs17597926
Exacrs17597926
Varsomers17597926
Maprs17597926
PheGenIrs17597926
hapmaprs17597926
1000 genomesrs17597926
hgdprs17597926
ensemblrs17597926
gopubmedrs17597926
geneviewrs17597926
scholarrs17597926
googlers17597926
pharmgkbrs17597926
gwascentralrs17597926
openSNPrs17597926
23andMers17597926
23andMe allrs17597926
SNP Nexus

SNPshotrs17597926
SNPdbers17597926
MSV3drs17597926
GWAS Ctlgrs17597926
GMAF0.01377
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 22451930OA-icon.png] Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating
GWAS snp
PMID [PMID 22688191OA-icon.png]
Trait
Title Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Risk Allele
P-val 1E-7
Odds Ratio 1.3600 None