rs10998466
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10998466(A;G) |
| Make rs10998466(G;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 68866673 |
| Gene | STOX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10998466 |
| dbSNP (classic) | rs10998466 |
| ClinGen | rs10998466 |
| ebi | rs10998466 |
| HLI | rs10998466 |
| Exac | rs10998466 |
| Gnomad | rs10998466 |
| Varsome | rs10998466 |
| LitVar | rs10998466 |
| Map | rs10998466 |
| PheGenI | rs10998466 |
| Biobank | rs10998466 |
| 1000 genomes | rs10998466 |
| hgdp | rs10998466 |
| ensembl | rs10998466 |
| geneview | rs10998466 |
| scholar | rs10998466 |
| rs10998466 | |
| pharmgkb | rs10998466 |
| gwascentral | rs10998466 |
| openSNP | rs10998466 |
| 23andMe | rs10998466 |
| SNPshot | rs10998466 |
| SNPdbe | rs10998466 |
| MSV3d | rs10998466 |
| GWAS Ctlg | rs10998466 |
| GMAF | 0.03581 |
| 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 | A |
| P-val | 4E-6 |
| Odds Ratio | .53 [0.31-0.75] unit decrease |
