rs926849
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs926849(A;A) |
| Make rs926849(A;G) |
| Make rs926849(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 161740587 |
| Gene | PARK2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs926849 |
| dbSNP (classic) | rs926849 |
| ClinGen | rs926849 |
| ebi | rs926849 |
| HLI | rs926849 |
| Exac | rs926849 |
| Gnomad | rs926849 |
| Varsome | rs926849 |
| LitVar | rs926849 |
| Map | rs926849 |
| PheGenI | rs926849 |
| Biobank | rs926849 |
| 1000 genomes | rs926849 |
| hgdp | rs926849 |
| ensembl | rs926849 |
| geneview | rs926849 |
| scholar | rs926849 |
| rs926849 | |
| pharmgkb | rs926849 |
| gwascentral | rs926849 |
| openSNP | rs926849 |
| 23andMe | rs926849 |
| SNPshot | rs926849 |
| SNPdbe | rs926849 |
| MSV3d | rs926849 |
| GWAS Ctlg | rs926849 |
| GMAF | 0.2741 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 22993228 ]
|
| Trait | Disc degeneration (lumbar) |
| Title | Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects. |
| Risk Allele | C |
| P-val | 3E-8 |
| Odds Ratio | .13 [0.083-0.177] unit decrease |
