rs3138053
| Orientation | minus |
| Stabilized | minus |
| Make rs3138053(A;A) |
| Make rs3138053(A;G) |
| Make rs3138053(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 14 |
| Position | 35405648 |
| Gene | NFKBIA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3138053 |
| dbSNP (classic) | rs3138053 |
| ClinGen | rs3138053 |
| ebi | rs3138053 |
| HLI | rs3138053 |
| Exac | rs3138053 |
| Gnomad | rs3138053 |
| Varsome | rs3138053 |
| LitVar | rs3138053 |
| Map | rs3138053 |
| PheGenI | rs3138053 |
| Biobank | rs3138053 |
| 1000 genomes | rs3138053 |
| hgdp | rs3138053 |
| ensembl | rs3138053 |
| geneview | rs3138053 |
| scholar | rs3138053 |
| rs3138053 | |
| pharmgkb | rs3138053 |
| gwascentral | rs3138053 |
| openSNP | rs3138053 |
| 23andMe | rs3138053 |
| SNPshot | rs3138053 |
| SNPdbe | rs3138053 |
| MSV3d | rs3138053 |
| GWAS Ctlg | rs3138053 |
| GMAF | 0.2277 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 24368589] Inhibitor IκBα promoter functional polymorphisms in patients with multiple sclerosis
[PMID 17463416] IkappaB genetic polymorphisms and invasive pneumococcal disease.
[PMID 19500386
] Polymorphisms in NF-kappaB inhibitors and risk of epithelial ovarian cancer.
[PMID 19797428] IkappaBalpha gene promoter polymorphisms are associated with hepatocarcinogenesis in patients infected with hepatitis B virus genotype C.
[PMID 21274447] Genetic polymorphisms and posttraumatic complications.
[PMID 23487427] Functional genetic variation in NFKBIA and susceptibility to childhood asthma, bronchiolitis, and bronchopulmonary dysplasia.
[PMID 23996241] Gender-specific association of NFKBIA promoter polymorphisms with the risk of sporadic colorectal cancer
[PMID 25223483] Effect of functional nuclear factor kappaB genetic polymorphisms on hepatitis B virus persistence and their interactions with viral mutations on the risk of hepatocellular carcinoma
[PMID 26488500] Common Polymorphisms in the NFKBIA Gene and Cancer Susceptibility: A Meta-Analysis
[PMID 26885097] Association between genetic polymorphism in NFKB1 and NFKBIA and coronary artery disease in a Chinese Han population.
