rs223899
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs223899(A;A) |
| Make rs223899(A;C) |
| Make rs223899(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 16 |
| Position | 57410664 |
| Gene | CCL17 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs223899 |
| dbSNP (classic) | rs223899 |
| ClinGen | rs223899 |
| ebi | rs223899 |
| HLI | rs223899 |
| Exac | rs223899 |
| Gnomad | rs223899 |
| Varsome | rs223899 |
| LitVar | rs223899 |
| Map | rs223899 |
| PheGenI | rs223899 |
| Biobank | rs223899 |
| 1000 genomes | rs223899 |
| hgdp | rs223899 |
| ensembl | rs223899 |
| geneview | rs223899 |
| scholar | rs223899 |
| rs223899 | |
| pharmgkb | rs223899 |
| gwascentral | rs223899 |
| openSNP | rs223899 |
| 23andMe | rs223899 |
| SNPshot | rs223899 |
| SNPdbe | rs223899 |
| MSV3d | rs223899 |
| GWAS Ctlg | rs223899 |
| GMAF | 0.2553 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
|
| ||
[PMID 23920401] Genetic variants in nuclear factor-kappa B binding sites are associated with clinical outcomes in prostate cancer patients
[PMID 26182268] [Association of single nucleotide polymorphisms in TARC/CCL17 gene with Kawasaki disease and its clinical characteristics]
