rs7179456
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7179456(G;G) |
| Make rs7179456(G;T) |
| Make rs7179456(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 58882340 |
| Gene | SLTM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7179456 |
| dbSNP (classic) | rs7179456 |
| ClinGen | rs7179456 |
| ebi | rs7179456 |
| HLI | rs7179456 |
| Exac | rs7179456 |
| Gnomad | rs7179456 |
| Varsome | rs7179456 |
| LitVar | rs7179456 |
| Map | rs7179456 |
| PheGenI | rs7179456 |
| Biobank | rs7179456 |
| 1000 genomes | rs7179456 |
| hgdp | rs7179456 |
| ensembl | rs7179456 |
| geneview | rs7179456 |
| scholar | rs7179456 |
| rs7179456 | |
| pharmgkb | rs7179456 |
| gwascentral | rs7179456 |
| openSNP | rs7179456 |
| 23andMe | rs7179456 |
| SNPshot | rs7179456 |
| SNPdbe | rs7179456 |
| MSV3d | rs7179456 |
| GWAS Ctlg | rs7179456 |
| GMAF | 0.4247 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21182207 ]
|
| Trait | |
| Title | Variants in several genomic regions associated with Asperger disorder |
| Risk Allele | |
| P-val | 0.000007 |
| Odds Ratio | None None |
