rs17750321
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17750321(A;A) |
| Make rs17750321(A;C) |
| Make rs17750321(C;C) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 18 |
| Position | 37498719 |
| Gene | CELF4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17750321 |
| dbSNP (classic) | rs17750321 |
| ClinGen | rs17750321 |
| ebi | rs17750321 |
| HLI | rs17750321 |
| Exac | rs17750321 |
| Gnomad | rs17750321 |
| Varsome | rs17750321 |
| LitVar | rs17750321 |
| Map | rs17750321 |
| PheGenI | rs17750321 |
| Biobank | rs17750321 |
| 1000 genomes | rs17750321 |
| hgdp | rs17750321 |
| ensembl | rs17750321 |
| geneview | rs17750321 |
| scholar | rs17750321 |
| rs17750321 | |
| pharmgkb | rs17750321 |
| gwascentral | rs17750321 |
| openSNP | rs17750321 |
| 23andMe | rs17750321 |
| SNPshot | rs17750321 |
| SNPdbe | rs17750321 |
| MSV3d | rs17750321 |
| GWAS Ctlg | rs17750321 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | A |
| P-val | 5E-6 |
| Odds Ratio | .30 [0.18-0.42] unit increase |
