rs28362459
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs28362459(G;G) |
| Make rs28362459(G;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 19 |
| Position | 5844781 |
| Gene | FUT3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs28362459 |
| dbSNP (classic) | rs28362459 |
| ClinGen | rs28362459 |
| ebi | rs28362459 |
| HLI | rs28362459 |
| Exac | rs28362459 |
| Gnomad | rs28362459 |
| Varsome | rs28362459 |
| LitVar | rs28362459 |
| Map | rs28362459 |
| PheGenI | rs28362459 |
| Biobank | rs28362459 |
| 1000 genomes | rs28362459 |
| hgdp | rs28362459 |
| ensembl | rs28362459 |
| geneview | rs28362459 |
| scholar | rs28362459 |
| rs28362459 | |
| pharmgkb | rs28362459 |
| gwascentral | rs28362459 |
| openSNP | rs28362459 |
| 23andMe | rs28362459 |
| SNPshot | rs28362459 |
| SNPdbe | rs28362459 |
| MSV3d | rs28362459 |
| GWAS Ctlg | rs28362459 |
| GMAF | 0.2089 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs28362459(A;A) rs28362459(G;G) |
| Alt | rs28362459(A;A) rs28362459(G;G) |
| Reference | Rs28362459(T;T) |
| Significance | Other |
| Disease | Le(-) PHENOTYPE |
| Variation | info |
| Gene | FUT3 |
| CLNDBN | Le(-) PHENOTYPE |
| Reversed | 1 |
| HGVS | NC_000019.9:g.5844792A>C |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000019289.23, |
[PMID 19169360
] Histo-blood group gene polymorphisms as potential genetic modifiers of infection and cystic fibrosis lung disease severity.
