Rs4431523
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4431523 |
| PheGenI | rs4431523 |
| nextbio | rs4431523 |
| hapmap | rs4431523 |
| 1000 genomes | rs4431523 |
| hgdp | rs4431523 |
| ensembl | rs4431523 |
| gopubmed | rs4431523 |
| geneview | rs4431523 |
| scholar | rs4431523 |
| rs4431523 | |
| pharmgkb | rs4431523 |
| gwascentral | rs4431523 |
| openSNP | rs4431523 |
| 23andMe | rs4431523 |
| 23andMe all | rs4431523 |
| SNP Nexus | |
| SNPshot | rs4431523 |
| SNPdbe | rs4431523 |
| MSV3d | rs4431523 |
| Gene | CNTNAP2 |
| Chromosome | 7 |
| Orientation | plus |
| GMAF | 0.2601 |
| Position | 147597166 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs4431523(C;C) |
| Make rs4431523(C;T) |
| Make rs4431523(T;T) |
news rs4431523 in CNTNAP2 were significantly associated with the inability of children with typical specific language impairment to process and repeat nonsense words
NEJM 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)
[PMID 18987363] A functional genetic link between distinct developmental language disorders.
