rs1788229
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1788229(A;A) |
| Make rs1788229(A;C) |
| Make rs1788229(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 69866725 |
| Gene | CD226 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1788229 |
| dbSNP (classic) | rs1788229 |
| ClinGen | rs1788229 |
| ebi | rs1788229 |
| HLI | rs1788229 |
| Exac | rs1788229 |
| Gnomad | rs1788229 |
| Varsome | rs1788229 |
| LitVar | rs1788229 |
| Map | rs1788229 |
| PheGenI | rs1788229 |
| Biobank | rs1788229 |
| 1000 genomes | rs1788229 |
| hgdp | rs1788229 |
| ensembl | rs1788229 |
| geneview | rs1788229 |
| scholar | rs1788229 |
| rs1788229 | |
| pharmgkb | rs1788229 |
| gwascentral | rs1788229 |
| openSNP | rs1788229 |
| 23andMe | rs1788229 |
| SNPshot | rs1788229 |
| SNPdbe | rs1788229 |
| MSV3d | rs1788229 |
| GWAS Ctlg | rs1788229 |
| GMAF | 0.4725 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 23922043] Lack of association between CD226 genetic variants and inflammatory demyelinating diseases in Korean population
