rs315949
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs315949(C;C) |
| Make rs315949(C;T) |
| Make rs315949(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 113135197 |
| Gene | IL1RN |
| is a | snp |
| is | mentioned by |
| dbSNP | rs315949 |
| dbSNP (classic) | rs315949 |
| ClinGen | rs315949 |
| ebi | rs315949 |
| HLI | rs315949 |
| Exac | rs315949 |
| Gnomad | rs315949 |
| Varsome | rs315949 |
| LitVar | rs315949 |
| Map | rs315949 |
| PheGenI | rs315949 |
| Biobank | rs315949 |
| 1000 genomes | rs315949 |
| hgdp | rs315949 |
| ensembl | rs315949 |
| geneview | rs315949 |
| scholar | rs315949 |
| rs315949 | |
| pharmgkb | rs315949 |
| gwascentral | rs315949 |
| openSNP | rs315949 |
| 23andMe | rs315949 |
| SNPshot | rs315949 |
| SNPdbe | rs315949 |
| MSV3d | rs315949 |
| GWAS Ctlg | rs315949 |
| GMAF | 0.2847 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 20178882] Genetic variation of the interleukin-1 family and nongenetic factors determining the interleukin-1 receptor antagonist phenotypes
[PMID 19729864
] Association of genetic variation in serum amyloid-A with cardiovascular disease and interactions with IL6, IL1RN, IL1beta and TNF genes in the Cardiovascular Health Study.
