rs10488
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs10488(A;A) |
| Make rs10488(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 102797291 |
| Gene | MMP1, WTAPP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10488 |
| dbSNP (classic) | rs10488 |
| ClinGen | rs10488 |
| ebi | rs10488 |
| HLI | rs10488 |
| Exac | rs10488 |
| Gnomad | rs10488 |
| Varsome | rs10488 |
| LitVar | rs10488 |
| Map | rs10488 |
| PheGenI | rs10488 |
| Biobank | rs10488 |
| 1000 genomes | rs10488 |
| hgdp | rs10488 |
| ensembl | rs10488 |
| geneview | rs10488 |
| scholar | rs10488 |
| rs10488 | |
| pharmgkb | rs10488 |
| gwascentral | rs10488 |
| openSNP | rs10488 |
| 23andMe | rs10488 |
| SNPshot | rs10488 |
| SNPdbe | rs10488 |
| MSV3d | rs10488 |
| GWAS Ctlg | rs10488 |
| GMAF | 0.07163 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23077567
] Assessment of the association of matrix metalloproteinases with myopia, refractive error and ocular biometric measures in an Australian cohort
[PMID 20078883] Association of MMP-2 polymorphisms with severe and very severe COPD: a case control study of MMPs-1, 9 and 12 in a European population.
| ClinVar | |
|---|---|
| Risk | rs10488(A;A) |
| Alt | rs10488(A;A) |
| Reference | Rs10488(G;G) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | MMP1 WTAPP1 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000011.9:g.102668022C>T |
| CLNSRC | |
| CLNACC | RCV000454871.1, |
