rs17225178
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17225178(A;A) |
| Make rs17225178(A;T) |
| Make rs17225178(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 15 |
| Position | 80451525 |
| Gene | ARNT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17225178 |
| dbSNP (classic) | rs17225178 |
| ClinGen | rs17225178 |
| ebi | rs17225178 |
| HLI | rs17225178 |
| Exac | rs17225178 |
| Gnomad | rs17225178 |
| Varsome | rs17225178 |
| LitVar | rs17225178 |
| Map | rs17225178 |
| PheGenI | rs17225178 |
| Biobank | rs17225178 |
| 1000 genomes | rs17225178 |
| hgdp | rs17225178 |
| ensembl | rs17225178 |
| geneview | rs17225178 |
| scholar | rs17225178 |
| rs17225178 | |
| pharmgkb | rs17225178 |
| gwascentral | rs17225178 |
| openSNP | rs17225178 |
| 23andMe | rs17225178 |
| SNPshot | rs17225178 |
| SNPdbe | rs17225178 |
| MSV3d | rs17225178 |
| GWAS Ctlg | rs17225178 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25745553
] Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome
