rs2361689
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2361689(C;C) |
Make rs2361689(C;T) |
Make rs2361689(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 155462637 |
Gene | EN2 |
is a | snp |
is | mentioned by |
dbSNP | rs2361689 |
dbSNP (classic) | rs2361689 |
ClinGen | rs2361689 |
ebi | rs2361689 |
HLI | rs2361689 |
Exac | rs2361689 |
Gnomad | rs2361689 |
Varsome | rs2361689 |
LitVar | rs2361689 |
Map | rs2361689 |
PheGenI | rs2361689 |
Biobank | rs2361689 |
1000 genomes | rs2361689 |
hgdp | rs2361689 |
ensembl | rs2361689 |
geneview | rs2361689 |
scholar | rs2361689 |
rs2361689 | |
pharmgkb | rs2361689 |
gwascentral | rs2361689 |
openSNP | rs2361689 |
23andMe | rs2361689 |
SNPshot | rs2361689 |
SNPdbe | rs2361689 |
MSV3d | rs2361689 |
GWAS Ctlg | rs2361689 |
GMAF | 0.3499 |
Max Magnitude | 0 |
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[PMID 15024396] Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder.
[PMID 16252243] Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.