rs6602175
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6602175(G;G) |
| Make rs6602175(G;T) |
| Make rs6602175(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 17100527 |
| Gene | CUBN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6602175 |
| dbSNP (classic) | rs6602175 |
| ClinGen | rs6602175 |
| ebi | rs6602175 |
| HLI | rs6602175 |
| Exac | rs6602175 |
| Gnomad | rs6602175 |
| Varsome | rs6602175 |
| LitVar | rs6602175 |
| Map | rs6602175 |
| PheGenI | rs6602175 |
| Biobank | rs6602175 |
| 1000 genomes | rs6602175 |
| hgdp | rs6602175 |
| ensembl | rs6602175 |
| geneview | rs6602175 |
| scholar | rs6602175 |
| rs6602175 | |
| pharmgkb | rs6602175 |
| gwascentral | rs6602175 |
| openSNP | rs6602175 |
| 23andMe | rs6602175 |
| SNPshot | rs6602175 |
| SNPdbe | rs6602175 |
| MSV3d | rs6602175 |
| GWAS Ctlg | rs6602175 |
| GMAF | 0.4197 |
| Max Magnitude | 0 |
| ? | (G;G) (G;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21116278 ]
|
| Trait | |
| Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
| Risk Allele | |
| P-val | 0.000003 |
| Odds Ratio | 0.0075 [NR] unit decrease (main effect) |
[PMID 31770575] Association between CUBN gene variants, type 2 diabetes and vitamin D concentrations in an elderly Greek population.
