rs2228149
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs2228149(C;T) |
| Make rs2228149(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 10 |
| Position | 6021545 |
| Gene | IL2RA |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2228149 |
| dbSNP (classic) | rs2228149 |
| ClinGen | rs2228149 |
| ebi | rs2228149 |
| HLI | rs2228149 |
| Exac | rs2228149 |
| Gnomad | rs2228149 |
| Varsome | rs2228149 |
| LitVar | rs2228149 |
| Map | rs2228149 |
| PheGenI | rs2228149 |
| Biobank | rs2228149 |
| 1000 genomes | rs2228149 |
| hgdp | rs2228149 |
| ensembl | rs2228149 |
| geneview | rs2228149 |
| scholar | rs2228149 |
| rs2228149 | |
| pharmgkb | rs2228149 |
| gwascentral | rs2228149 |
| openSNP | rs2228149 |
| 23andMe | rs2228149 |
| SNPshot | rs2228149 |
| SNPdbe | rs2228149 |
| MSV3d | rs2228149 |
| GWAS Ctlg | rs2228149 |
| GMAF | 0.06336 |
| Max Magnitude | 0 |
[PMID 21239413] Association of IL2RA polymorphisms with susceptibility to multiple sclerosis is not explained by missense mutations in IL2RA
[PMID 16385451
] A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease.
[PMID 18715339] Associations between cytokine/cytokine receptor single nucleotide polymorphisms and humoral immunity to measles, mumps and rubella in a Somali population.
| ClinVar | |
|---|---|
| Risk | rs2228149(T;T) |
| Alt | rs2228149(T;T) |
| Reference | Rs2228149(C;C) |
| Significance | Non-pathogenic |
| Disease | Interleukin 2 receptor |
| Variation | info |
| Gene | IL2RA |
| CLNDBN | Interleukin 2 receptor, alpha, deficiency of |
| Reversed | 1 |
| HGVS | NC_000010.10:g.6063508G>A |
| CLNSRC | |
| CLNACC | RCV000262595.1, |
