rs2021786
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2021786(A;A) |
| Make rs2021786(A;G) |
| Make rs2021786(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 20 |
| Position | 17441333 |
| Gene | PCSK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2021786 |
| dbSNP (classic) | rs2021786 |
| ClinGen | rs2021786 |
| ebi | rs2021786 |
| HLI | rs2021786 |
| Exac | rs2021786 |
| Gnomad | rs2021786 |
| Varsome | rs2021786 |
| LitVar | rs2021786 |
| Map | rs2021786 |
| PheGenI | rs2021786 |
| Biobank | rs2021786 |
| 1000 genomes | rs2021786 |
| hgdp | rs2021786 |
| ensembl | rs2021786 |
| geneview | rs2021786 |
| scholar | rs2021786 |
| rs2021786 | |
| pharmgkb | rs2021786 |
| gwascentral | rs2021786 |
| openSNP | rs2021786 |
| 23andMe | rs2021786 |
| SNPshot | rs2021786 |
| SNPdbe | rs2021786 |
| MSV3d | rs2021786 |
| GWAS Ctlg | rs2021786 |
| Max Magnitude | 0 |
| GWAS snp | |
|---|---|
| PMID | [PMID 24839885] |
| Trait | Preschool internalizing problems |
| Title | A genome-wide association meta-analysis of preschool internalizing problems. |
| Risk Allele | T |
| P-val | 7E-6 |
| Odds Ratio | .10 [0.058-0.15] unit decrease |
