rs10790289
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs10790289(C;C) |
| Make rs10790289(C;T) |
| Make rs10790289(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 119344455 |
| Gene | C1QTNF5, MFRP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10790289 |
| dbSNP (classic) | rs10790289 |
| ClinGen | rs10790289 |
| ebi | rs10790289 |
| HLI | rs10790289 |
| Exac | rs10790289 |
| Gnomad | rs10790289 |
| Varsome | rs10790289 |
| LitVar | rs10790289 |
| Map | rs10790289 |
| PheGenI | rs10790289 |
| Biobank | rs10790289 |
| 1000 genomes | rs10790289 |
| hgdp | rs10790289 |
| ensembl | rs10790289 |
| geneview | rs10790289 |
| scholar | rs10790289 |
| rs10790289 | |
| pharmgkb | rs10790289 |
| gwascentral | rs10790289 |
| openSNP | rs10790289 |
| 23andMe | rs10790289 |
| SNPshot | rs10790289 |
| SNPdbe | rs10790289 |
| MSV3d | rs10790289 |
| GWAS Ctlg | rs10790289 |
| GMAF | 0.489 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22933837
] A cross-ethnicity investigation of genes previously implicated in primary angle closure glaucoma
[PMID 18334955] Common MFRP sequence variants are not associated with moderate to high hyperopia, isolated microphthalmia, and high myopia.
[PMID 18781223] The association of membrane frizzled-related protein (MFRP) gene with acute angle-closure glaucoma--a pilot study.
