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rs2228946

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2228946(A;A)
Make rs2228946(A;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position117278031
GeneWNT2
is asnp
is mentioned by
dbSNPrs2228946
ebirs2228946
HLIrs2228946
Exacrs2228946
Varsomers2228946
Maprs2228946
PheGenIrs2228946
hapmaprs2228946
1000 genomesrs2228946
hgdprs2228946
ensemblrs2228946
gopubmedrs2228946
geneviewrs2228946
scholarrs2228946
googlers2228946
pharmgkbrs2228946
gwascentralrs2228946
openSNPrs2228946
23andMers2228946
23andMe allrs2228946
SNP Nexus

SNPshotrs2228946
SNPdbers2228946
MSV3drs2228946
GWAS Ctlgrs2228946
GMAF0.1919
Max Magnitude0
? (A;A) (A;G) (G;G) 28

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


[PMID 19838307OA-icon.png] Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes.