rs2017567
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2017567(C;C) |
| Make rs2017567(C;T) |
| Make rs2017567(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 587212 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2017567 |
| dbSNP (classic) | rs2017567 |
| ClinGen | rs2017567 |
| ebi | rs2017567 |
| HLI | rs2017567 |
| Exac | rs2017567 |
| Gnomad | rs2017567 |
| Varsome | rs2017567 |
| LitVar | rs2017567 |
| Map | rs2017567 |
| PheGenI | rs2017567 |
| Biobank | rs2017567 |
| 1000 genomes | rs2017567 |
| hgdp | rs2017567 |
| ensembl | rs2017567 |
| geneview | rs2017567 |
| scholar | rs2017567 |
| rs2017567 | |
| pharmgkb | rs2017567 |
| gwascentral | rs2017567 |
| openSNP | rs2017567 |
| 23andMe | rs2017567 |
| SNPshot | rs2017567 |
| SNPdbe | rs2017567 |
| MSV3d | rs2017567 |
| GWAS Ctlg | rs2017567 |
| GMAF | 0.478 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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 | C |
| P-val | 9E-6 |
| Odds Ratio | .10 [0.059-0.141] unit increase |
