rs104886474
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs104886474(C;C) |
| Make rs104886474(C;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 7 |
| Position | 151181424 |
| Gene | ASB10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs104886474 |
| dbSNP (classic) | rs104886474 |
| ClinGen | rs104886474 |
| ebi | rs104886474 |
| HLI | rs104886474 |
| Exac | rs104886474 |
| Gnomad | rs104886474 |
| Varsome | rs104886474 |
| LitVar | rs104886474 |
| Map | rs104886474 |
| PheGenI | rs104886474 |
| Biobank | rs104886474 |
| 1000 genomes | rs104886474 |
| hgdp | rs104886474 |
| ensembl | rs104886474 |
| geneview | rs104886474 |
| scholar | rs104886474 |
| rs104886474 | |
| pharmgkb | rs104886474 |
| gwascentral | rs104886474 |
| openSNP | rs104886474 |
| 23andMe | rs104886474 |
| SNPshot | rs104886474 |
| SNPdbe | rs104886474 |
| MSV3d | rs104886474 |
| GWAS Ctlg | rs104886474 |
| GMAF | 0.0009183 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs104886474(C;C) |
| Alt | rs104886474(C;C) |
| Reference | Rs104886474(G;G) |
| Significance | Pathogenic |
| Disease | Glaucoma 1 |
| Variation | info |
| Gene | ASB10 |
| CLNDBN | Glaucoma 1, open angle, F |
| Reversed | 1 |
| HGVS | NC_000007.13:g.150878511C>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000043658.3, |
[PMID 10037570] GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36.
