rs1006113
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1006113(A;A) |
| Make rs1006113(A;G) |
| Make rs1006113(G;G) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 4 |
| Position | 8388584 |
| Gene | ACOX3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1006113 |
| dbSNP (classic) | rs1006113 |
| ClinGen | rs1006113 |
| ebi | rs1006113 |
| HLI | rs1006113 |
| Exac | rs1006113 |
| Gnomad | rs1006113 |
| Varsome | rs1006113 |
| LitVar | rs1006113 |
| Map | rs1006113 |
| PheGenI | rs1006113 |
| Biobank | rs1006113 |
| 1000 genomes | rs1006113 |
| hgdp | rs1006113 |
| ensembl | rs1006113 |
| geneview | rs1006113 |
| scholar | rs1006113 |
| rs1006113 | |
| pharmgkb | rs1006113 |
| gwascentral | rs1006113 |
| openSNP | rs1006113 |
| 23andMe | rs1006113 |
| SNPshot | rs1006113 |
| SNPdbe | rs1006113 |
| MSV3d | rs1006113 |
| GWAS Ctlg | rs1006113 |
| Max Magnitude | 0 |
[PMID 27552335] The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency.
