rs980238
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs980238(A;A) |
| Make rs980238(A;C) |
| Make rs980238(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 8 |
| Position | 4425096 |
| Gene | CSMD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs980238 |
| dbSNP (classic) | rs980238 |
| ClinGen | rs980238 |
| ebi | rs980238 |
| HLI | rs980238 |
| Exac | rs980238 |
| Gnomad | rs980238 |
| Varsome | rs980238 |
| LitVar | rs980238 |
| Map | rs980238 |
| PheGenI | rs980238 |
| Biobank | rs980238 |
| 1000 genomes | rs980238 |
| hgdp | rs980238 |
| ensembl | rs980238 |
| geneview | rs980238 |
| scholar | rs980238 |
| rs980238 | |
| pharmgkb | rs980238 |
| gwascentral | rs980238 |
| openSNP | rs980238 |
| 23andMe | rs980238 |
| SNPshot | rs980238 |
| SNPdbe | rs980238 |
| MSV3d | rs980238 |
| GWAS Ctlg | rs980238 |
| GMAF | 0.3728 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 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 | 9E-6 |
| Odds Ratio | .10 [0.055-0.145] unit decrease |
