rs2396753
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2396753(A;A) |
| Make rs2396753(A;C) |
| Make rs2396753(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 114508276 |
| Gene | FOXP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2396753 |
| dbSNP (classic) | rs2396753 |
| ClinGen | rs2396753 |
| ebi | rs2396753 |
| HLI | rs2396753 |
| Exac | rs2396753 |
| Gnomad | rs2396753 |
| Varsome | rs2396753 |
| LitVar | rs2396753 |
| Map | rs2396753 |
| PheGenI | rs2396753 |
| Biobank | rs2396753 |
| 1000 genomes | rs2396753 |
| hgdp | rs2396753 |
| ensembl | rs2396753 |
| geneview | rs2396753 |
| scholar | rs2396753 |
| rs2396753 | |
| pharmgkb | rs2396753 |
| gwascentral | rs2396753 |
| openSNP | rs2396753 |
| 23andMe | rs2396753 |
| SNPshot | rs2396753 |
| SNPdbe | rs2396753 |
| MSV3d | rs2396753 |
| GWAS Ctlg | rs2396753 |
| GMAF | 0.371 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 21334420] rs2396753 (C>A) gene variant of the FOXP2 gene has significant effects on grey matter concentration in patients with schizophrenia.
[PMID 16538183] Association between FOXP2 polymorphisms and schizophrenia with auditory hallucinations.
[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.
