rs2484992
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common genotype |
| Make rs2484992(A;A) |
| Make rs2484992(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 31223169 |
| Gene | LOC101929352 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2484992 |
| dbSNP (classic) | rs2484992 |
| ClinGen | rs2484992 |
| ebi | rs2484992 |
| HLI | rs2484992 |
| Exac | rs2484992 |
| Gnomad | rs2484992 |
| Varsome | rs2484992 |
| LitVar | rs2484992 |
| Map | rs2484992 |
| PheGenI | rs2484992 |
| Biobank | rs2484992 |
| 1000 genomes | rs2484992 |
| hgdp | rs2484992 |
| ensembl | rs2484992 |
| geneview | rs2484992 |
| scholar | rs2484992 |
| rs2484992 | |
| pharmgkb | rs2484992 |
| gwascentral | rs2484992 |
| openSNP | rs2484992 |
| 23andMe | rs2484992 |
| SNPshot | rs2484992 |
| SNPdbe | rs2484992 |
| MSV3d | rs2484992 |
| GWAS Ctlg | rs2484992 |
| GMAF | 0.2374 |
| 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 | C |
| P-val | 5E-6 |
| Odds Ratio | .68 [0.39-0.97] unit increase |
