rs10214886
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10214886(A;A) |
| Make rs10214886(A;T) |
| Make rs10214886(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32889642 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10214886 |
| dbSNP (classic) | rs10214886 |
| ClinGen | rs10214886 |
| ebi | rs10214886 |
| HLI | rs10214886 |
| Exac | rs10214886 |
| Gnomad | rs10214886 |
| Varsome | rs10214886 |
| LitVar | rs10214886 |
| Map | rs10214886 |
| PheGenI | rs10214886 |
| Biobank | rs10214886 |
| 1000 genomes | rs10214886 |
| hgdp | rs10214886 |
| ensembl | rs10214886 |
| geneview | rs10214886 |
| scholar | rs10214886 |
| rs10214886 | |
| pharmgkb | rs10214886 |
| gwascentral | rs10214886 |
| openSNP | rs10214886 |
| 23andMe | rs10214886 |
| SNPshot | rs10214886 |
| SNPdbe | rs10214886 |
| MSV3d | rs10214886 |
| GWAS Ctlg | rs10214886 |
| GMAF | 0.1272 |
| Max Magnitude | 0 |
| ? | (A;A) (A;T) (T;T) | 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 | 2E-7 |
| Odds Ratio | .19 [0.12-0.26] unit increase |
