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rs4730775

From SNPedia

Orientationplus
Stabilizedplus
Make rs4730775(C;C)
Make rs4730775(C;T)
Make rs4730775(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117277064
GeneWNT2
is asnp
is mentioned by
dbSNPrs4730775
ebirs4730775
HLIrs4730775
Exacrs4730775
Varsomers4730775
Maprs4730775
PheGenIrs4730775
hapmaprs4730775
1000 genomesrs4730775
hgdprs4730775
ensemblrs4730775
gopubmedrs4730775
geneviewrs4730775
scholarrs4730775
googlers4730775
pharmgkbrs4730775
gwascentralrs4730775
openSNPrs4730775
23andMers4730775
23andMe allrs4730775
SNP Nexus

SNPshotrs4730775
SNPdbers4730775
MSV3drs4730775
GWAS Ctlgrs4730775
GMAF0.3545
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21732829]
Trait
Title Wnt signaling and Dupuytren's disease.
Risk Allele
P-val 3E-8
Odds Ratio 1.2000 None


[PMID 20492734OA-icon.png] No association between polymorphisms of WNT2 and schizophrenia in a Korean population.


[PMID 20626912OA-icon.png] Association between polymorphisms of arachidonate 12-lipoxygenase (ALOX12) and schizophrenia in a Korean population.


[PMID 22489561] WNT2 Locus Is Involved in Genetic Susceptibility of Peyronie's Disease.