rs1053839
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1053839(C;C) |
| Make rs1053839(C;T) |
| Make rs1053839(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 18814110 |
| Gene | C20orf78, SCP2D1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1053839 |
| dbSNP (classic) | rs1053839 |
| ClinGen | rs1053839 |
| ebi | rs1053839 |
| HLI | rs1053839 |
| Exac | rs1053839 |
| Gnomad | rs1053839 |
| Varsome | rs1053839 |
| LitVar | rs1053839 |
| Map | rs1053839 |
| PheGenI | rs1053839 |
| Biobank | rs1053839 |
| 1000 genomes | rs1053839 |
| hgdp | rs1053839 |
| ensembl | rs1053839 |
| geneview | rs1053839 |
| scholar | rs1053839 |
| rs1053839 | |
| pharmgkb | rs1053839 |
| gwascentral | rs1053839 |
| openSNP | rs1053839 |
| 23andMe | rs1053839 |
| SNPshot | rs1053839 |
| SNPdbe | rs1053839 |
| MSV3d | rs1053839 |
| GWAS Ctlg | rs1053839 |
| GMAF | 0.2006 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19574904
] Exclusion of Positional Candidate Gene Coding Region Mutations in the Common Posterior Polymorphous Corneal Dystrophy 1 Candidate Gene Interval
