rs10227893
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs10227893(G;G) |
| Make rs10227893(G;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 114630022 |
| Gene | FOXP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10227893 |
| dbSNP (classic) | rs10227893 |
| ClinGen | rs10227893 |
| ebi | rs10227893 |
| HLI | rs10227893 |
| Exac | rs10227893 |
| Gnomad | rs10227893 |
| Varsome | rs10227893 |
| LitVar | rs10227893 |
| Map | rs10227893 |
| PheGenI | rs10227893 |
| Biobank | rs10227893 |
| 1000 genomes | rs10227893 |
| hgdp | rs10227893 |
| ensembl | rs10227893 |
| geneview | rs10227893 |
| scholar | rs10227893 |
| rs10227893 | |
| pharmgkb | rs10227893 |
| gwascentral | rs10227893 |
| openSNP | rs10227893 |
| 23andMe | rs10227893 |
| SNPshot | rs10227893 |
| SNPdbe | rs10227893 |
| MSV3d | rs10227893 |
| GWAS Ctlg | rs10227893 |
| GMAF | 0.118 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 15877281
] variations in rs17137124 and rs10227893 may impair speech
| ClinVar | |
|---|---|
| Risk | rs10227893(A;A) rs10227893(G;G) |
| Alt | rs10227893(A;A) rs10227893(G;G) |
| Reference | Rs10227893(T;T) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | FOXP2 |
| CLNDBN | not specified |
| Reversed | 0 |
| HGVS | NC_000007.13:g.114270077T>G |
| CLNSRC | ClinVar |
| CLNACC | RCV000081645.4, |
