rs1345514
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1345514(C;C) |
| Make rs1345514(C;T) |
| Make rs1345514(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 155456455 |
| Gene | EN2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1345514 |
| dbSNP (classic) | rs1345514 |
| ClinGen | rs1345514 |
| ebi | rs1345514 |
| HLI | rs1345514 |
| Exac | rs1345514 |
| Gnomad | rs1345514 |
| Varsome | rs1345514 |
| LitVar | rs1345514 |
| Map | rs1345514 |
| PheGenI | rs1345514 |
| Biobank | rs1345514 |
| 1000 genomes | rs1345514 |
| hgdp | rs1345514 |
| ensembl | rs1345514 |
| geneview | rs1345514 |
| scholar | rs1345514 |
| rs1345514 | |
| pharmgkb | rs1345514 |
| gwascentral | rs1345514 |
| openSNP | rs1345514 |
| 23andMe | rs1345514 |
| SNPshot | rs1345514 |
| SNPdbe | rs1345514 |
| MSV3d | rs1345514 |
| GWAS Ctlg | rs1345514 |
| GMAF | 0.2227 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19270442] Haplotype analysis of the engrailed-2 gene in young-onset Parkinson's disease
[PMID 16252243
] Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.
