rs3024067
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3024067(A;A) |
Make rs3024067(A;C) |
Make rs3024067(C;C) |
Reference | GRCm38 38.1/137 |
Chromosome | 4 |
Position | 26732277 |
is a | snp |
is | mentioned by |
dbSNP | rs3024067 |
dbSNP (classic) | rs3024067 |
ClinGen | rs3024067 |
ebi | rs3024067 |
HLI | rs3024067 |
Exac | rs3024067 |
Gnomad | rs3024067 |
Varsome | rs3024067 |
LitVar | rs3024067 |
Map | rs3024067 |
PheGenI | rs3024067 |
Biobank | rs3024067 |
1000 genomes | rs3024067 |
hgdp | rs3024067 |
ensembl | rs3024067 |
geneview | rs3024067 |
scholar | rs3024067 |
rs3024067 | |
pharmgkb | rs3024067 |
gwascentral | rs3024067 |
openSNP | rs3024067 |
23andMe | rs3024067 |
SNPshot | rs3024067 |
SNPdbe | rs3024067 |
MSV3d | rs3024067 |
GWAS Ctlg | rs3024067 |
Max Magnitude | 0 |
[PMID 20523082] Intronic single nucleotide polymorphisms of engrailed homeobox 2 modulate the disease vulnerability of autism in a han chinese population