rs4703129
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4703129(A;A) |
| Make rs4703129(A;C) |
| Make rs4703129(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 98553032 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4703129 |
| dbSNP (classic) | rs4703129 |
| ClinGen | rs4703129 |
| ebi | rs4703129 |
| HLI | rs4703129 |
| Exac | rs4703129 |
| Gnomad | rs4703129 |
| Varsome | rs4703129 |
| LitVar | rs4703129 |
| Map | rs4703129 |
| PheGenI | rs4703129 |
| Biobank | rs4703129 |
| 1000 genomes | rs4703129 |
| hgdp | rs4703129 |
| ensembl | rs4703129 |
| geneview | rs4703129 |
| scholar | rs4703129 |
| rs4703129 | |
| pharmgkb | rs4703129 |
| gwascentral | rs4703129 |
| openSNP | rs4703129 |
| 23andMe | rs4703129 |
| SNPshot | rs4703129 |
| SNPdbe | rs4703129 |
| MSV3d | rs4703129 |
| GWAS Ctlg | rs4703129 |
| GMAF | 0.3985 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21182207 ]
|
| Trait | |
| Title | Variants in several genomic regions associated with Asperger disorder |
| Risk Allele | |
| P-val | 0.000001 |
| Odds Ratio | None None |
