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rs17594526

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17594526(C;T)
Make rs17594526(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position55391007
GeneTCF4
is asnp
is mentioned by
dbSNPrs17594526
ebirs17594526
HLIrs17594526
Exacrs17594526
Varsomers17594526
Maprs17594526
PheGenIrs17594526
hapmaprs17594526
1000 genomesrs17594526
hgdprs17594526
ensemblrs17594526
gopubmedrs17594526
geneviewrs17594526
scholarrs17594526
googlers17594526
pharmgkbrs17594526
gwascentralrs17594526
openSNPrs17594526
23andMers17594526
23andMe allrs17594526
SNP Nexus

SNPshotrs17594526
SNPdbers17594526
MSV3drs17594526
GWAS Ctlgrs17594526
GMAF0.05601
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19571811OA-icon.png]
Trait Schizophrenia
Title Common polygenic variation contributes to risk of schizophrenia and bipolar disorder
Risk Allele T
P-val 1E-7
Odds Ratio 1.44 None


GET Evidence
rs17594526
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary