rs2184971
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs2184971(C;C) |
| Make rs2184971(C;T) |
| Make rs2184971(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 100165838 |
| Gene | PCCA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2184971 |
| dbSNP (classic) | rs2184971 |
| ClinGen | rs2184971 |
| ebi | rs2184971 |
| HLI | rs2184971 |
| Exac | rs2184971 |
| Gnomad | rs2184971 |
| Varsome | rs2184971 |
| LitVar | rs2184971 |
| Map | rs2184971 |
| PheGenI | rs2184971 |
| Biobank | rs2184971 |
| 1000 genomes | rs2184971 |
| hgdp | rs2184971 |
| ensembl | rs2184971 |
| geneview | rs2184971 |
| scholar | rs2184971 |
| rs2184971 | |
| pharmgkb | rs2184971 |
| gwascentral | rs2184971 |
| openSNP | rs2184971 |
| 23andMe | rs2184971 |
| SNPshot | rs2184971 |
| SNPdbe | rs2184971 |
| MSV3d | rs2184971 |
| GWAS Ctlg | rs2184971 |
| GMAF | 0.4486 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23396134 ]
|
| Trait | Refractive error |
| Title | Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. |
| Risk Allele | G |
| P-val | 2E-8 |
| Odds Ratio | .09 [0.056-0.114] unit increase |
