rs7704909
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7704909(C;C) |
| Make rs7704909(C;T) |
| Make rs7704909(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 25898812 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7704909 |
| dbSNP (classic) | rs7704909 |
| ClinGen | rs7704909 |
| ebi | rs7704909 |
| HLI | rs7704909 |
| Exac | rs7704909 |
| Gnomad | rs7704909 |
| Varsome | rs7704909 |
| LitVar | rs7704909 |
| Map | rs7704909 |
| PheGenI | rs7704909 |
| Biobank | rs7704909 |
| 1000 genomes | rs7704909 |
| hgdp | rs7704909 |
| ensembl | rs7704909 |
| geneview | rs7704909 |
| scholar | rs7704909 |
| rs7704909 | |
| pharmgkb | rs7704909 |
| gwascentral | rs7704909 |
| openSNP | rs7704909 |
| 23andMe | rs7704909 |
| SNPshot | rs7704909 |
| SNPdbe | rs7704909 |
| MSV3d | rs7704909 |
| GWAS Ctlg | rs7704909 |
| GMAF | 0.2392 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19456320
] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
