rs151344606
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs151344606(A;A) |
| Make rs151344606(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 151186412 |
| Gene | ASB10 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs151344606 |
| dbSNP (classic) | rs151344606 |
| ClinGen | rs151344606 |
| ebi | rs151344606 |
| HLI | rs151344606 |
| Exac | rs151344606 |
| Gnomad | rs151344606 |
| Varsome | rs151344606 |
| LitVar | rs151344606 |
| Map | rs151344606 |
| PheGenI | rs151344606 |
| Biobank | rs151344606 |
| 1000 genomes | rs151344606 |
| hgdp | rs151344606 |
| ensembl | rs151344606 |
| geneview | rs151344606 |
| scholar | rs151344606 |
| rs151344606 | |
| pharmgkb | rs151344606 |
| gwascentral | rs151344606 |
| openSNP | rs151344606 |
| 23andMe | rs151344606 |
| SNPshot | rs151344606 |
| SNPdbe | rs151344606 |
| MSV3d | rs151344606 |
| GWAS Ctlg | rs151344606 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs151344606(A;A) |
| Alt | rs151344606(A;A) |
| Reference | Rs151344606(C;C) |
| Significance | Pathogenic |
| Disease | Glaucoma 1 |
| Variation | info |
| Gene | ASB10 |
| CLNDBN | Glaucoma 1, open angle, F |
| Reversed | 1 |
| HGVS | NC_000007.13:g.150883499G>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000043657.3, |
[PMID 10037570] GLC1F, a new primary open-angle glaucoma locus, maps to 7q35-q36.
