rs17137124
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17137124(C;C) |
| Make rs17137124(C;T) |
| Make rs17137124(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 114570759 |
| Gene | FOXP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17137124 |
| dbSNP (classic) | rs17137124 |
| ClinGen | rs17137124 |
| ebi | rs17137124 |
| HLI | rs17137124 |
| Exac | rs17137124 |
| Gnomad | rs17137124 |
| Varsome | rs17137124 |
| LitVar | rs17137124 |
| Map | rs17137124 |
| PheGenI | rs17137124 |
| Biobank | rs17137124 |
| 1000 genomes | rs17137124 |
| hgdp | rs17137124 |
| ensembl | rs17137124 |
| geneview | rs17137124 |
| scholar | rs17137124 |
| rs17137124 | |
| pharmgkb | rs17137124 |
| gwascentral | rs17137124 |
| openSNP | rs17137124 |
| 23andMe | rs17137124 |
| SNPshot | rs17137124 |
| SNPdbe | rs17137124 |
| MSV3d | rs17137124 |
| GWAS Ctlg | rs17137124 |
| GMAF | 0.4692 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 15877281
] variations in rs17137124 and rs10227893 may impair speech
[PMID 22129783] FOXP2, APOE, and PRNP: New Modulators in Primary Progressive Aphasia
[PMID 19997522] Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment.
[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.
