rs3774937
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs3774937(C;C) |
| Make rs3774937(C;T) |
| Make rs3774937(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 4 |
| Position | 102513096 |
| Gene | NFKB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3774937 |
| dbSNP (classic) | rs3774937 |
| ClinGen | rs3774937 |
| ebi | rs3774937 |
| HLI | rs3774937 |
| Exac | rs3774937 |
| Gnomad | rs3774937 |
| Varsome | rs3774937 |
| LitVar | rs3774937 |
| Map | rs3774937 |
| PheGenI | rs3774937 |
| Biobank | rs3774937 |
| 1000 genomes | rs3774937 |
| hgdp | rs3774937 |
| ensembl | rs3774937 |
| geneview | rs3774937 |
| scholar | rs3774937 |
| rs3774937 | |
| pharmgkb | rs3774937 |
| gwascentral | rs3774937 |
| openSNP | rs3774937 |
| 23andMe | rs3774937 |
| SNPshot | rs3774937 |
| SNPdbe | rs3774937 |
| MSV3d | rs3774937 |
| GWAS Ctlg | rs3774937 |
| GMAF | 0.292 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 23153769] Impact of NF-κB gene polymorphism on allograft outcome in Hispanic renal transplant recipients
[PMID 19223558
] Polymorphic variation in NFKB1 and other aspirin-related genes and risk of Hodgkin lymphoma.
[PMID 25397881] Intronic Variants in the NFKB1 Gene May Influence Hearing Forecast in Patients with Unilateral Sensorineural Hearing Loss in Meniere's Disease
