rs201649896
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs201649896(A;T) |
| Make rs201649896(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 7 |
| Position | 114426561 |
| Gene | FOXP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs201649896 |
| dbSNP (classic) | rs201649896 |
| ClinGen | rs201649896 |
| ebi | rs201649896 |
| HLI | rs201649896 |
| Exac | rs201649896 |
| Gnomad | rs201649896 |
| Varsome | rs201649896 |
| LitVar | rs201649896 |
| Map | rs201649896 |
| PheGenI | rs201649896 |
| Biobank | rs201649896 |
| 1000 genomes | rs201649896 |
| hgdp | rs201649896 |
| ensembl | rs201649896 |
| geneview | rs201649896 |
| scholar | rs201649896 |
| rs201649896 | |
| pharmgkb | rs201649896 |
| gwascentral | rs201649896 |
| openSNP | rs201649896 |
| 23andMe | rs201649896 |
| SNPshot | rs201649896 |
| SNPdbe | rs201649896 |
| MSV3d | rs201649896 |
| GWAS Ctlg | rs201649896 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs201649896(T;T) |
| Alt | rs201649896(T;T) |
| Reference | Rs201649896(A;A) |
| Significance | Other |
| Disease | not specified Speech-language disorder 1 |
| Variation | info |
| Gene | FOXP2 |
| CLNDBN | not specified Speech-language disorder 1 |
| Reversed | 0 |
| HGVS | NC_000007.13:g.114066616A>T |
| CLNSRC | |
| CLNACC | RCV000175859.1, RCV000234933.2, |
