rs714816
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs714816(C;C) |
| Make rs714816(C;T) |
| Make rs714816(T;T) |
| Reference | GRCh38.p2 38.2/147 |
| Chromosome | 10 |
| Position | 122496829 |
| Gene | HTRA1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs714816 |
| dbSNP (classic) | rs714816 |
| ClinGen | rs714816 |
| ebi | rs714816 |
| HLI | rs714816 |
| Exac | rs714816 |
| Gnomad | rs714816 |
| Varsome | rs714816 |
| LitVar | rs714816 |
| Map | rs714816 |
| PheGenI | rs714816 |
| Biobank | rs714816 |
| 1000 genomes | rs714816 |
| hgdp | rs714816 |
| ensembl | rs714816 |
| geneview | rs714816 |
| scholar | rs714816 |
| rs714816 | |
| pharmgkb | rs714816 |
| gwascentral | rs714816 |
| openSNP | rs714816 |
| 23andMe | rs714816 |
| SNPshot | rs714816 |
| SNPdbe | rs714816 |
| MSV3d | rs714816 |
| GWAS Ctlg | rs714816 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 27416785
] Analysis of copy number variation at DMBT1 and age-related macular degeneration.
