rs35678
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs35678(C;C) |
| Make rs35678(C;T) |
| Make rs35678(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 10338239 |
| Gene | ATP2B2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35678 |
| dbSNP (classic) | rs35678 |
| ClinGen | rs35678 |
| ebi | rs35678 |
| HLI | rs35678 |
| Exac | rs35678 |
| Gnomad | rs35678 |
| Varsome | rs35678 |
| LitVar | rs35678 |
| Map | rs35678 |
| PheGenI | rs35678 |
| Biobank | rs35678 |
| 1000 genomes | rs35678 |
| hgdp | rs35678 |
| ensembl | rs35678 |
| geneview | rs35678 |
| scholar | rs35678 |
| rs35678 | |
| pharmgkb | rs35678 |
| gwascentral | rs35678 |
| openSNP | rs35678 |
| 23andMe | rs35678 |
| SNPshot | rs35678 |
| SNPdbe | rs35678 |
| MSV3d | rs35678 |
| GWAS Ctlg | rs35678 |
| GMAF | 0.4734 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22739633] The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families
[PMID 20678243
] Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.
