rs4778137
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs4778137(C;C) |
| Make rs4778137(C;G) |
| Make rs4778137(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 28082689 |
| Gene | OCA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4778137 |
| dbSNP (classic) | rs4778137 |
| ClinGen | rs4778137 |
| ebi | rs4778137 |
| HLI | rs4778137 |
| Exac | rs4778137 |
| Gnomad | rs4778137 |
| Varsome | rs4778137 |
| LitVar | rs4778137 |
| Map | rs4778137 |
| PheGenI | rs4778137 |
| Biobank | rs4778137 |
| 1000 genomes | rs4778137 |
| hgdp | rs4778137 |
| ensembl | rs4778137 |
| geneview | rs4778137 |
| scholar | rs4778137 |
| rs4778137 | |
| pharmgkb | rs4778137 |
| gwascentral | rs4778137 |
| openSNP | rs4778137 |
| 23andMe | rs4778137 |
| SNPshot | rs4778137 |
| SNPdbe | rs4778137 |
| MSV3d | rs4778137 |
| GWAS Ctlg | rs4778137 |
| GMAF | 0.4674 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 20308648
] Association Between a Germline OCA2 Polymorphism at Chromosome 15q13.1 and Estrogen Receptor-Negative Breast Cancer Survival
[PMID 17236130] A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation.
[PMID 18252221] Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.
