rs16831128
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs16831128(A;G) |
| Make rs16831128(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 132386819 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs16831128 |
| dbSNP (classic) | rs16831128 |
| ClinGen | rs16831128 |
| ebi | rs16831128 |
| HLI | rs16831128 |
| Exac | rs16831128 |
| Gnomad | rs16831128 |
| Varsome | rs16831128 |
| LitVar | rs16831128 |
| Map | rs16831128 |
| PheGenI | rs16831128 |
| Biobank | rs16831128 |
| 1000 genomes | rs16831128 |
| hgdp | rs16831128 |
| ensembl | rs16831128 |
| geneview | rs16831128 |
| scholar | rs16831128 |
| rs16831128 | |
| pharmgkb | rs16831128 |
| gwascentral | rs16831128 |
| openSNP | rs16831128 |
| 23andMe | rs16831128 |
| SNPshot | rs16831128 |
| SNPdbe | rs16831128 |
| MSV3d | rs16831128 |
| GWAS Ctlg | rs16831128 |
| GMAF | 0.1974 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585324 ]
|
| Trait | Conduct disorder (case status) |
| Title | Genome-wide association study of conduct disorder symptomatology |
| Risk Allele | |
| P-val | 4E-7 |
| Odds Ratio | 1.45 [1.26-1.67] |
