rs6750486
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6750486(C;C) |
| Make rs6750486(C;T) |
| Make rs6750486(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 35301852 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6750486 |
| dbSNP (classic) | rs6750486 |
| ClinGen | rs6750486 |
| ebi | rs6750486 |
| HLI | rs6750486 |
| Exac | rs6750486 |
| Gnomad | rs6750486 |
| Varsome | rs6750486 |
| LitVar | rs6750486 |
| Map | rs6750486 |
| PheGenI | rs6750486 |
| Biobank | rs6750486 |
| 1000 genomes | rs6750486 |
| hgdp | rs6750486 |
| ensembl | rs6750486 |
| geneview | rs6750486 |
| scholar | rs6750486 |
| rs6750486 | |
| pharmgkb | rs6750486 |
| gwascentral | rs6750486 |
| openSNP | rs6750486 |
| 23andMe | rs6750486 |
| SNPshot | rs6750486 |
| SNPdbe | rs6750486 |
| MSV3d | rs6750486 |
| GWAS Ctlg | rs6750486 |
| GMAF | 0.1313 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20585324 ]
|
| Trait | Conduct disorder (symptom count) |
| Title | Genome-wide association study of conduct disorder symptomatology |
| Risk Allele | |
| P-val | 0.000006 |
| Odds Ratio | 0.10 [NR] unit increase |
