rs4622507
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4622507(C;C) |
| Make rs4622507(C;T) |
| Make rs4622507(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 55009755 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4622507 |
| dbSNP (classic) | rs4622507 |
| ClinGen | rs4622507 |
| ebi | rs4622507 |
| HLI | rs4622507 |
| Exac | rs4622507 |
| Gnomad | rs4622507 |
| Varsome | rs4622507 |
| LitVar | rs4622507 |
| Map | rs4622507 |
| PheGenI | rs4622507 |
| Biobank | rs4622507 |
| 1000 genomes | rs4622507 |
| hgdp | rs4622507 |
| ensembl | rs4622507 |
| geneview | rs4622507 |
| scholar | rs4622507 |
| rs4622507 | |
| pharmgkb | rs4622507 |
| gwascentral | rs4622507 |
| openSNP | rs4622507 |
| 23andMe | rs4622507 |
| SNPshot | rs4622507 |
| SNPdbe | rs4622507 |
| MSV3d | rs4622507 |
| GWAS Ctlg | rs4622507 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 24564958 ]
|
| Trait | Social communication problems |
| Title | Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence. |
| Risk Allele | C |
| P-val | 2E-6 |
| Odds Ratio | .15 [0.091-0.209] unit increase |
