rs6885224
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs6885224(C;C) |
| Make rs6885224(C;T) |
| Make rs6885224(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 11169833 |
| Gene | CTNND2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs6885224 |
| dbSNP (classic) | rs6885224 |
| ClinGen | rs6885224 |
| ebi | rs6885224 |
| HLI | rs6885224 |
| Exac | rs6885224 |
| Gnomad | rs6885224 |
| Varsome | rs6885224 |
| LitVar | rs6885224 |
| Map | rs6885224 |
| PheGenI | rs6885224 |
| Biobank | rs6885224 |
| 1000 genomes | rs6885224 |
| hgdp | rs6885224 |
| ensembl | rs6885224 |
| geneview | rs6885224 |
| scholar | rs6885224 |
| rs6885224 | |
| pharmgkb | rs6885224 |
| gwascentral | rs6885224 |
| openSNP | rs6885224 |
| 23andMe | rs6885224 |
| SNPshot | rs6885224 |
| SNPdbe | rs6885224 |
| MSV3d | rs6885224 |
| GWAS Ctlg | rs6885224 |
| GMAF | 0.3471 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 21095009 ]
|
| Trait | |
| Title | Genome-Wide Association Studies Reveal Genetic Variants in CTNND2 for High Myopia in Singapore Chinese |
| Risk Allele | C |
| P-val | 0.000008 |
| Odds Ratio | 1.2400 [1.11-1.39] |
[PMID 21911587] Replication study supports CTNND2 as a susceptibility gene for high myopia.
