rs3213787
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in complete genomics |
| Make rs3213787(A;G) |
| Make rs3213787(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 45419685 |
| Gene | SRBD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3213787 |
| dbSNP (classic) | rs3213787 |
| ClinGen | rs3213787 |
| ebi | rs3213787 |
| HLI | rs3213787 |
| Exac | rs3213787 |
| Gnomad | rs3213787 |
| Varsome | rs3213787 |
| LitVar | rs3213787 |
| Map | rs3213787 |
| PheGenI | rs3213787 |
| Biobank | rs3213787 |
| 1000 genomes | rs3213787 |
| hgdp | rs3213787 |
| ensembl | rs3213787 |
| geneview | rs3213787 |
| scholar | rs3213787 |
| rs3213787 | |
| pharmgkb | rs3213787 |
| gwascentral | rs3213787 |
| openSNP | rs3213787 |
| 23andMe | rs3213787 |
| SNPshot | rs3213787 |
| SNPdbe | rs3213787 |
| MSV3d | rs3213787 |
| GWAS Ctlg | rs3213787 |
| GMAF | 0.07254 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20363506] |
| Trait | Glaucoma |
| Title | Genome-wide Association Study of Normal Tension Glaucoma: Common Variants in SRBD1 and ELOVL5 Contribute to Disease Susceptibility |
| Risk Allele | A |
| P-val | 3E-9 |
| Odds Ratio | 2.80 [1.96-3.99] |
[PMID 22792221
] Common Variants on Chromosome 9p21 Are Associated with Normal Tension Glaucoma
[PMID 21508110] Association between SRBD1 and ELOVL5 gene polymorphisms and primary open-angle glaucoma.
