rs467691
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs467691(G;G) |
| Make rs467691(G;T) |
| Make rs467691(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 26914271 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs467691 |
| dbSNP (classic) | rs467691 |
| ClinGen | rs467691 |
| ebi | rs467691 |
| HLI | rs467691 |
| Exac | rs467691 |
| Gnomad | rs467691 |
| Varsome | rs467691 |
| LitVar | rs467691 |
| Map | rs467691 |
| PheGenI | rs467691 |
| Biobank | rs467691 |
| 1000 genomes | rs467691 |
| hgdp | rs467691 |
| ensembl | rs467691 |
| geneview | rs467691 |
| scholar | rs467691 |
| rs467691 | |
| pharmgkb | rs467691 |
| gwascentral | rs467691 |
| openSNP | rs467691 |
| 23andMe | rs467691 |
| SNPshot | rs467691 |
| SNPdbe | rs467691 |
| MSV3d | rs467691 |
| GWAS Ctlg | rs467691 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 23792102] Phenotype variations affect genetic association studies of degenerative disc disease: conclusions of analysis of genetic association of 58 single nucleotide polymorphisms with highly specific phenotypes for disc degeneration in 332 subjects
