rs3761168
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3761168(G;G) |
| Make rs3761168(G;T) |
| Make rs3761168(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 8885071 |
| Gene | PLCB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3761168 |
| dbSNP (classic) | rs3761168 |
| ClinGen | rs3761168 |
| ebi | rs3761168 |
| HLI | rs3761168 |
| Exac | rs3761168 |
| Gnomad | rs3761168 |
| Varsome | rs3761168 |
| LitVar | rs3761168 |
| Map | rs3761168 |
| PheGenI | rs3761168 |
| Biobank | rs3761168 |
| 1000 genomes | rs3761168 |
| hgdp | rs3761168 |
| ensembl | rs3761168 |
| geneview | rs3761168 |
| scholar | rs3761168 |
| rs3761168 | |
| pharmgkb | rs3761168 |
| gwascentral | rs3761168 |
| openSNP | rs3761168 |
| 23andMe | rs3761168 |
| SNPshot | rs3761168 |
| SNPdbe | rs3761168 |
| MSV3d | rs3761168 |
| GWAS Ctlg | rs3761168 |
| GMAF | 0.219 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24564958
] Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence
