rs1456031
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1456031(C;C) |
| Make rs1456031(C;T) |
| Make rs1456031(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 114656047 |
| Gene | FOXP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1456031 |
| dbSNP (classic) | rs1456031 |
| ClinGen | rs1456031 |
| ebi | rs1456031 |
| HLI | rs1456031 |
| Exac | rs1456031 |
| Gnomad | rs1456031 |
| Varsome | rs1456031 |
| LitVar | rs1456031 |
| Map | rs1456031 |
| PheGenI | rs1456031 |
| Biobank | rs1456031 |
| 1000 genomes | rs1456031 |
| hgdp | rs1456031 |
| ensembl | rs1456031 |
| geneview | rs1456031 |
| scholar | rs1456031 |
| rs1456031 | |
| pharmgkb | rs1456031 |
| gwascentral | rs1456031 |
| openSNP | rs1456031 |
| 23andMe | rs1456031 |
| SNPshot | rs1456031 |
| SNPdbe | rs1456031 |
| MSV3d | rs1456031 |
| GWAS Ctlg | rs1456031 |
| GMAF | 0.4284 |
| Max Magnitude | 0 |
[PMID 22129783] FOXP2, APOE, and PRNP: New Modulators in Primary Progressive Aphasia
[PMID 20649982
] FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.
[PMID 20858950] The speech and language FOXP2 gene modulates the phenotype of frontotemporal lobar degeneration.
[PMID 20923434] Association between FOXP2 gene and speech sound disorder in Chinese population.
