rs1859156
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1859156(G;G) |
| Make rs1859156(G;T) |
| Make rs1859156(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 94912883 |
| Gene | BMPR1B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1859156 |
| dbSNP (classic) | rs1859156 |
| ClinGen | rs1859156 |
| ebi | rs1859156 |
| HLI | rs1859156 |
| Exac | rs1859156 |
| Gnomad | rs1859156 |
| Varsome | rs1859156 |
| LitVar | rs1859156 |
| Map | rs1859156 |
| PheGenI | rs1859156 |
| Biobank | rs1859156 |
| 1000 genomes | rs1859156 |
| hgdp | rs1859156 |
| ensembl | rs1859156 |
| geneview | rs1859156 |
| scholar | rs1859156 |
| rs1859156 | |
| pharmgkb | rs1859156 |
| gwascentral | rs1859156 |
| openSNP | rs1859156 |
| 23andMe | rs1859156 |
| SNPshot | rs1859156 |
| SNPdbe | rs1859156 |
| MSV3d | rs1859156 |
| GWAS Ctlg | rs1859156 |
| GMAF | 0.2291 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20732626 ]
|
| Trait | |
| Title | Family-Based Genome-Wide Association Scan of Attention-Deficit/Hyperactivity Disorder |
| Risk Allele | |
| P-val | 0.000002 |
| Odds Ratio | 1.54 [NR] |
