rs3749982
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3749982(A;A) |
| Make rs3749982(A;T) |
| Make rs3749982(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32894830 |
| Gene | LOC100294145 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3749982 |
| dbSNP (classic) | rs3749982 |
| ClinGen | rs3749982 |
| ebi | rs3749982 |
| HLI | rs3749982 |
| Exac | rs3749982 |
| Gnomad | rs3749982 |
| Varsome | rs3749982 |
| LitVar | rs3749982 |
| Map | rs3749982 |
| PheGenI | rs3749982 |
| Biobank | rs3749982 |
| 1000 genomes | rs3749982 |
| hgdp | rs3749982 |
| ensembl | rs3749982 |
| geneview | rs3749982 |
| scholar | rs3749982 |
| rs3749982 | |
| pharmgkb | rs3749982 |
| gwascentral | rs3749982 |
| openSNP | rs3749982 |
| 23andMe | rs3749982 |
| SNPshot | rs3749982 |
| SNPdbe | rs3749982 |
| MSV3d | rs3749982 |
| GWAS Ctlg | rs3749982 |
| GMAF | 0.1129 |
| 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 | 1E-7 |
| Odds Ratio | .19 [0.12-0.26] unit increase |
