rs1428642
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1428642(A;A) |
| Make rs1428642(A;G) |
| Make rs1428642(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 53309270 |
| Gene | LOC107987270 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1428642 |
| dbSNP (classic) | rs1428642 |
| ClinGen | rs1428642 |
| ebi | rs1428642 |
| HLI | rs1428642 |
| Exac | rs1428642 |
| Gnomad | rs1428642 |
| Varsome | rs1428642 |
| LitVar | rs1428642 |
| Map | rs1428642 |
| PheGenI | rs1428642 |
| Biobank | rs1428642 |
| 1000 genomes | rs1428642 |
| hgdp | rs1428642 |
| ensembl | rs1428642 |
| geneview | rs1428642 |
| scholar | rs1428642 |
| rs1428642 | |
| pharmgkb | rs1428642 |
| gwascentral | rs1428642 |
| openSNP | rs1428642 |
| 23andMe | rs1428642 |
| SNPshot | rs1428642 |
| SNPdbe | rs1428642 |
| MSV3d | rs1428642 |
| GWAS Ctlg | rs1428642 |
| GMAF | 0.4867 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 21979947
] A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries
