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rs2896218

From SNPedia

Orientationplus
Stabilizedplus
Make rs2896218(A;A)
Make rs2896218(A;G)
Make rs2896218(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117279924
GeneWNT2
is asnp
is mentioned by
dbSNPrs2896218
ebirs2896218
HLIrs2896218
Exacrs2896218
Varsomers2896218
Maprs2896218
PheGenIrs2896218
hapmaprs2896218
1000 genomesrs2896218
hgdprs2896218
ensemblrs2896218
gopubmedrs2896218
geneviewrs2896218
scholarrs2896218
googlers2896218
pharmgkbrs2896218
gwascentralrs2896218
openSNPrs2896218
23andMers2896218
23andMe allrs2896218
SNP Nexus

SNPshotrs2896218
SNPdbers2896218
MSV3drs2896218
GWAS Ctlgrs2896218
GMAF0.3806
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 22522212] The WNT2 gene polymorphism associated with speech delay inherent to autism


[PMID 21575668] Association study of the CNS patterning genes and autism in Han Chinese in Taiwan.