rs10246256
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | None | |
| (C;T) | None | |
| (T;T) | higher risk of speech development delay and/or impairment |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 147857715 |
| Gene | CNTNAP2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10246256 |
| dbSNP (classic) | rs10246256 |
| ClinGen | rs10246256 |
| ebi | rs10246256 |
| HLI | rs10246256 |
| Exac | rs10246256 |
| Gnomad | rs10246256 |
| Varsome | rs10246256 |
| LitVar | rs10246256 |
| Map | rs10246256 |
| PheGenI | rs10246256 |
| Biobank | rs10246256 |
| 1000 genomes | rs10246256 |
| hgdp | rs10246256 |
| ensembl | rs10246256 |
| geneview | rs10246256 |
| scholar | rs10246256 |
| rs10246256 | |
| pharmgkb | rs10246256 |
| gwascentral | rs10246256 |
| openSNP | rs10246256 |
| 23andMe | rs10246256 |
| SNPshot | rs10246256 |
| SNPdbe | rs10246256 |
| MSV3d | rs10246256 |
| GWAS Ctlg | rs10246256 |
| GMAF | 0.2975 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 18987363
] Speech development rs4431523, rs17236239 and significant associations (with P values from 0.01 to 5.0x10–5) between nonsense-word repetition and nine intronic SNPs (rs851715, rs10246256, rs2710102, rs759178, rs1922892, rs2538991, rs17236239, rs2538976, and rs2710117)
