rs7744666
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7744666(C;C) |
| Make rs7744666(C;T) |
| Make rs7744666(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 6 |
| Position | 32891935 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7744666 |
| dbSNP (classic) | rs7744666 |
| ClinGen | rs7744666 |
| ebi | rs7744666 |
| HLI | rs7744666 |
| Exac | rs7744666 |
| Gnomad | rs7744666 |
| Varsome | rs7744666 |
| LitVar | rs7744666 |
| Map | rs7744666 |
| PheGenI | rs7744666 |
| Biobank | rs7744666 |
| 1000 genomes | rs7744666 |
| hgdp | rs7744666 |
| ensembl | rs7744666 |
| geneview | rs7744666 |
| scholar | rs7744666 |
| rs7744666 | |
| pharmgkb | rs7744666 |
| gwascentral | rs7744666 |
| openSNP | rs7744666 |
| 23andMe | rs7744666 |
| SNPshot | rs7744666 |
| SNPdbe | rs7744666 |
| MSV3d | rs7744666 |
| GWAS Ctlg | rs7744666 |
| GMAF | 0.1125 |
| 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 | 6E-8 |
| Odds Ratio | .20 [0.13-0.27] unit increase |
