rs1861046
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 1 |
| Make rs1861046(A;A) |
| Make rs1861046(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 15396282 |
| Gene | C1QTNF7, LOC101929095 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1861046 |
| dbSNP (classic) | rs1861046 |
| ClinGen | rs1861046 |
| ebi | rs1861046 |
| HLI | rs1861046 |
| Exac | rs1861046 |
| Gnomad | rs1861046 |
| Varsome | rs1861046 |
| LitVar | rs1861046 |
| Map | rs1861046 |
| PheGenI | rs1861046 |
| Biobank | rs1861046 |
| 1000 genomes | rs1861046 |
| hgdp | rs1861046 |
| ensembl | rs1861046 |
| geneview | rs1861046 |
| scholar | rs1861046 |
| rs1861046 | |
| pharmgkb | rs1861046 |
| gwascentral | rs1861046 |
| openSNP | rs1861046 |
| 23andMe | rs1861046 |
| SNPshot | rs1861046 |
| SNPdbe | rs1861046 |
| MSV3d | rs1861046 |
| GWAS Ctlg | rs1861046 |
| GMAF | 0.1478 |
| Max Magnitude | 1 |
| ? | (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 | 6E-8 |
| Odds Ratio | 1.65 [1.38-1.98] |
