rs878960
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs878960(A;A) |
| Make rs878960(A;G) |
| Make rs878960(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 26683789 |
| Gene | GABRB3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs878960 |
| dbSNP (classic) | rs878960 |
| ClinGen | rs878960 |
| ebi | rs878960 |
| HLI | rs878960 |
| Exac | rs878960 |
| Gnomad | rs878960 |
| Varsome | rs878960 |
| LitVar | rs878960 |
| Map | rs878960 |
| PheGenI | rs878960 |
| Biobank | rs878960 |
| 1000 genomes | rs878960 |
| hgdp | rs878960 |
| ensembl | rs878960 |
| geneview | rs878960 |
| scholar | rs878960 |
| rs878960 | |
| pharmgkb | rs878960 |
| gwascentral | rs878960 |
| openSNP | rs878960 |
| 23andMe | rs878960 |
| SNPshot | rs878960 |
| SNPdbe | rs878960 |
| MSV3d | rs878960 |
| GWAS Ctlg | rs878960 |
| GMAF | 0.4913 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21786105
] Single nucleotide polymorphisms predict symptom severity of autism spectrum disorder
[PMID 18978678
] Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts.
[PMID 22037176] Predictive models for subtypes of autism spectrum disorder based on single-nucleotide polymorphisms and magnetic resonance imaging.
