rs4149579
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 1 | Tumor Necrosis Factor 1A Receptor Intron Variant Homozygous |
| (G;G) | 0 | common in complete genomics |
| Make rs4149579(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 6338191 |
| Gene | TNFRSF1A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4149579 |
| dbSNP (classic) | rs4149579 |
| ClinGen | rs4149579 |
| ebi | rs4149579 |
| HLI | rs4149579 |
| Exac | rs4149579 |
| Gnomad | rs4149579 |
| Varsome | rs4149579 |
| LitVar | rs4149579 |
| Map | rs4149579 |
| PheGenI | rs4149579 |
| Biobank | rs4149579 |
| 1000 genomes | rs4149579 |
| hgdp | rs4149579 |
| ensembl | rs4149579 |
| geneview | rs4149579 |
| scholar | rs4149579 |
| rs4149579 | |
| pharmgkb | rs4149579 |
| gwascentral | rs4149579 |
| openSNP | rs4149579 |
| 23andMe | rs4149579 |
| SNPshot | rs4149579 |
| SNPdbe | rs4149579 |
| MSV3d | rs4149579 |
| GWAS Ctlg | rs4149579 |
| GMAF | 0.03535 |
| Max Magnitude | 1 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
c.39+3585G>A is a rare SNV in an intronic region of TNFRSF1A, the gene for tumor necrosis factor receptor 1A.
[PMID 21212151
] Interactions Between Genetic Polymorphisms in the Apoptotic Pathway and Environmental Factors on Esophageal Adenocarcinoma Risk
