rs2209852
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2209852(A;A) |
| Make rs2209852(A;G) |
| Make rs2209852(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 13 |
| Position | 94865368 |
| Gene | LOC101927284 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2209852 |
| dbSNP (classic) | rs2209852 |
| ClinGen | rs2209852 |
| ebi | rs2209852 |
| HLI | rs2209852 |
| Exac | rs2209852 |
| Gnomad | rs2209852 |
| Varsome | rs2209852 |
| LitVar | rs2209852 |
| Map | rs2209852 |
| PheGenI | rs2209852 |
| Biobank | rs2209852 |
| 1000 genomes | rs2209852 |
| hgdp | rs2209852 |
| ensembl | rs2209852 |
| geneview | rs2209852 |
| scholar | rs2209852 |
| rs2209852 | |
| pharmgkb | rs2209852 |
| gwascentral | rs2209852 |
| openSNP | rs2209852 |
| 23andMe | rs2209852 |
| SNPshot | rs2209852 |
| SNPdbe | rs2209852 |
| MSV3d | rs2209852 |
| GWAS Ctlg | rs2209852 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24571439 ]
|
| Trait | Parent of origin effect on language impairment (paternal) |
| Title | Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. |
| Risk Allele | |
| P-val | 6E-6 |
| Odds Ratio | NR NR |
