rs3757385
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs3757385(A;A) |
| Make rs3757385(A;C) |
| Make rs3757385(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 128937250 |
| Gene | IRF5 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs3757385 |
| dbSNP (classic) | rs3757385 |
| ClinGen | rs3757385 |
| ebi | rs3757385 |
| HLI | rs3757385 |
| Exac | rs3757385 |
| Gnomad | rs3757385 |
| Varsome | rs3757385 |
| LitVar | rs3757385 |
| Map | rs3757385 |
| PheGenI | rs3757385 |
| Biobank | rs3757385 |
| 1000 genomes | rs3757385 |
| hgdp | rs3757385 |
| ensembl | rs3757385 |
| geneview | rs3757385 |
| scholar | rs3757385 |
| rs3757385 | |
| pharmgkb | rs3757385 |
| gwascentral | rs3757385 |
| openSNP | rs3757385 |
| 23andMe | rs3757385 |
| SNPshot | rs3757385 |
| SNPdbe | rs3757385 |
| MSV3d | rs3757385 |
| GWAS Ctlg | rs3757385 |
| GMAF | 0.4968 |
| Max Magnitude | 0 |
| ? | (A;A) (A;C) (C;C) | 28 |
|---|---|---|
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| ||
[PMID 20980283] The interferon regulatory factor 5 gene confers susceptibility to rheumatoid arthritis and influences its erosive phenotype
[PMID 18285424
] Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations.
[PMID 20231204] Phenotype-haplotype correlation of IRF5 in systemic sclerosis: role of 2 haplotypes in disease severity.
[PMID 24788560] Genetic Polymorphism of Interferon Regulatory Factor 5 (IRF5) Correlates with Allograft Acute Rejection of Liver Transplantation
