rs5906883
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs5906883(A;A) |
| Make rs5906883(A;C) |
| Make rs5906883(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 43667695 |
| Gene | MAOA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs5906883 |
| dbSNP (classic) | rs5906883 |
| ClinGen | rs5906883 |
| ebi | rs5906883 |
| HLI | rs5906883 |
| Exac | rs5906883 |
| Gnomad | rs5906883 |
| Varsome | rs5906883 |
| LitVar | rs5906883 |
| Map | rs5906883 |
| PheGenI | rs5906883 |
| Biobank | rs5906883 |
| 1000 genomes | rs5906883 |
| hgdp | rs5906883 |
| ensembl | rs5906883 |
| geneview | rs5906883 |
| scholar | rs5906883 |
| rs5906883 | |
| pharmgkb | rs5906883 |
| gwascentral | rs5906883 |
| openSNP | rs5906883 |
| 23andMe | rs5906883 |
| SNPshot | rs5906883 |
| SNPdbe | rs5906883 |
| MSV3d | rs5906883 |
| GWAS Ctlg | rs5906883 |
| GMAF | 0.4329 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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| ||
[PMID 19100789] Family- and population-based association studies of monoamine oxidase A and autism spectrum disorders in Korean
