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rs3024067

From SNPedia

Orientationminus
Stabilizedminus
Make rs3024067(A;A)
Make rs3024067(A;C)
Make rs3024067(C;C)
ReferenceGRCm38 38.1/137
Chromosome4
Position26732277
is asnp
is mentioned by
dbSNPrs3024067
ebirs3024067
HLIrs3024067
Exacrs3024067
Varsomers3024067
Maprs3024067
PheGenIrs3024067
hapmaprs3024067
1000 genomesrs3024067
hgdprs3024067
ensemblrs3024067
gopubmedrs3024067
geneviewrs3024067
scholarrs3024067
googlers3024067
pharmgkbrs3024067
gwascentralrs3024067
openSNPrs3024067
23andMers3024067
23andMe allrs3024067
SNP Nexus

SNPshotrs3024067
SNPdbers3024067
MSV3drs3024067
GWAS Ctlgrs3024067
Max Magnitude

[PMID 20523082] Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population