rs1042631
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1042631(C;C) |
| Make rs1042631(C;T) |
| Make rs1042631(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 88859008 |
| Gene | ACAN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1042631 |
| dbSNP (classic) | rs1042631 |
| ClinGen | rs1042631 |
| ebi | rs1042631 |
| HLI | rs1042631 |
| Exac | rs1042631 |
| Gnomad | rs1042631 |
| Varsome | rs1042631 |
| LitVar | rs1042631 |
| Map | rs1042631 |
| PheGenI | rs1042631 |
| Biobank | rs1042631 |
| 1000 genomes | rs1042631 |
| hgdp | rs1042631 |
| ensembl | rs1042631 |
| geneview | rs1042631 |
| scholar | rs1042631 |
| rs1042631 | |
| pharmgkb | rs1042631 |
| gwascentral | rs1042631 |
| openSNP | rs1042631 |
| 23andMe | rs1042631 |
| SNPshot | rs1042631 |
| SNPdbe | rs1042631 |
| MSV3d | rs1042631 |
| GWAS Ctlg | rs1042631 |
| Max Magnitude | 0 |
| ? | (C;C) (C;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
