rs3759222
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3759222(A;A) |
| Make rs3759222(A;C) |
| Make rs3759222(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 91113176 |
| Gene | LUM |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3759222 |
| dbSNP (classic) | rs3759222 |
| ClinGen | rs3759222 |
| ebi | rs3759222 |
| HLI | rs3759222 |
| Exac | rs3759222 |
| Gnomad | rs3759222 |
| Varsome | rs3759222 |
| LitVar | rs3759222 |
| Map | rs3759222 |
| PheGenI | rs3759222 |
| Biobank | rs3759222 |
| 1000 genomes | rs3759222 |
| hgdp | rs3759222 |
| ensembl | rs3759222 |
| geneview | rs3759222 |
| scholar | rs3759222 |
| rs3759222 | |
| pharmgkb | rs3759222 |
| gwascentral | rs3759222 |
| openSNP | rs3759222 |
| 23andMe | rs3759222 |
| SNPshot | rs3759222 |
| SNPdbe | rs3759222 |
| MSV3d | rs3759222 |
| GWAS Ctlg | rs3759222 |
| GMAF | 0.3104 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 23145541] Absence of an association between lumican promoter variants and high myopia in the Korean population
