rs2233406
Orientation | minus |
Stabilized | minus |
Make rs2233406(C;C) |
Make rs2233406(C;T) |
Make rs2233406(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 35405593 |
Gene | NFKBIA |
is a | snp |
is | mentioned by |
dbSNP | rs2233406 |
dbSNP (classic) | rs2233406 |
ClinGen | rs2233406 |
ebi | rs2233406 |
HLI | rs2233406 |
Exac | rs2233406 |
Gnomad | rs2233406 |
Varsome | rs2233406 |
LitVar | rs2233406 |
Map | rs2233406 |
PheGenI | rs2233406 |
Biobank | rs2233406 |
1000 genomes | rs2233406 |
hgdp | rs2233406 |
ensembl | rs2233406 |
geneview | rs2233406 |
scholar | rs2233406 |
rs2233406 | |
pharmgkb | rs2233406 |
gwascentral | rs2233406 |
openSNP | rs2233406 |
23andMe | rs2233406 |
SNPshot | rs2233406 |
SNPdbe | rs2233406 |
MSV3d | rs2233406 |
GWAS Ctlg | rs2233406 |
GMAF | 0.2277 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24368589] Inhibitor IκBα promoter functional polymorphisms in patients with multiple sclerosis
[PMID 17463416] IkappaB genetic polymorphisms and invasive pneumococcal disease.
[PMID 19797428] IkappaBalpha gene promoter polymorphisms are associated with hepatocarcinogenesis in patients infected with hepatitis B virus genotype C.
[PMID 19886988] Association of polymorphism in genes encoding kappaB inhibitors (IkappaB) with susceptibility to and phenotype of Graves' disease: a case-control study.
[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.