rs10895322
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs10895322(A;G) |
| Make rs10895322(G;G) |
| Reference | GRCh38.p2 38.2/144 |
| Chromosome | 11 |
| Position | 102599525 |
| Gene | MMP20 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10895322 |
| dbSNP (classic) | rs10895322 |
| ClinGen | rs10895322 |
| ebi | rs10895322 |
| HLI | rs10895322 |
| Exac | rs10895322 |
| Gnomad | rs10895322 |
| Varsome | rs10895322 |
| LitVar | rs10895322 |
| Map | rs10895322 |
| PheGenI | rs10895322 |
| Biobank | rs10895322 |
| 1000 genomes | rs10895322 |
| hgdp | rs10895322 |
| ensembl | rs10895322 |
| geneview | rs10895322 |
| scholar | rs10895322 |
| rs10895322 | |
| pharmgkb | rs10895322 |
| gwascentral | rs10895322 |
| openSNP | rs10895322 |
| 23andMe | rs10895322 |
| SNPshot | rs10895322 |
| SNPdbe | rs10895322 |
| MSV3d | rs10895322 |
| GWAS Ctlg | rs10895322 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 26337002] MMP20 and ARMS2/HTRA1 Are Associated with Neovascular Lesion Size in Age-Related Macular Degeneration
| ClinVar | |
|---|---|
| Risk | rs10895322(G;G) |
| Alt | rs10895322(G;G) |
| Reference | Rs10895322(A;A) |
| Significance | Untested |
| Disease | not provided |
| Variation | info |
| Gene | MMP20 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.102470256A>G |
| CLNSRC | |
| CLNACC | RCV000190296.1, |
