rs1474526
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1474526(C;C) |
| Make rs1474526(C;T) |
| Make rs1474526(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 10 |
| Position | 122446128 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1474526 |
| dbSNP (classic) | rs1474526 |
| ClinGen | rs1474526 |
| ebi | rs1474526 |
| HLI | rs1474526 |
| Exac | rs1474526 |
| Gnomad | rs1474526 |
| Varsome | rs1474526 |
| LitVar | rs1474526 |
| Map | rs1474526 |
| PheGenI | rs1474526 |
| Biobank | rs1474526 |
| 1000 genomes | rs1474526 |
| hgdp | rs1474526 |
| ensembl | rs1474526 |
| geneview | rs1474526 |
| scholar | rs1474526 |
| rs1474526 | |
| pharmgkb | rs1474526 |
| gwascentral | rs1474526 |
| openSNP | rs1474526 |
| 23andMe | rs1474526 |
| SNPshot | rs1474526 |
| SNPdbe | rs1474526 |
| MSV3d | rs1474526 |
| GWAS Ctlg | rs1474526 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 27416785
] Analysis of copy number variation at DMBT1 and age-related macular degeneration.
