rs7199390
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7199390(A;A) |
| Make rs7199390(A;T) |
| Make rs7199390(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 16 |
| Position | 11219194 |
| Gene | LOC107984859 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7199390 |
| dbSNP (classic) | rs7199390 |
| ClinGen | rs7199390 |
| ebi | rs7199390 |
| HLI | rs7199390 |
| Exac | rs7199390 |
| Gnomad | rs7199390 |
| Varsome | rs7199390 |
| LitVar | rs7199390 |
| Map | rs7199390 |
| PheGenI | rs7199390 |
| Biobank | rs7199390 |
| 1000 genomes | rs7199390 |
| hgdp | rs7199390 |
| ensembl | rs7199390 |
| geneview | rs7199390 |
| scholar | rs7199390 |
| rs7199390 | |
| pharmgkb | rs7199390 |
| gwascentral | rs7199390 |
| openSNP | rs7199390 |
| 23andMe | rs7199390 |
| SNPshot | rs7199390 |
| SNPdbe | rs7199390 |
| MSV3d | rs7199390 |
| GWAS Ctlg | rs7199390 |
| Max Magnitude | 0 |
| ? | (A;A) (A;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 | T |
| P-val | 2E-6 |
| Odds Ratio | .19 [0.11-0.27] unit increase |
