rs10491434
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs10491434(C;C) |
| Make rs10491434(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 35877812 |
| Gene | IL7R |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10491434 |
| dbSNP (classic) | rs10491434 |
| ClinGen | rs10491434 |
| ebi | rs10491434 |
| HLI | rs10491434 |
| Exac | rs10491434 |
| Gnomad | rs10491434 |
| Varsome | rs10491434 |
| LitVar | rs10491434 |
| Map | rs10491434 |
| PheGenI | rs10491434 |
| Biobank | rs10491434 |
| 1000 genomes | rs10491434 |
| hgdp | rs10491434 |
| ensembl | rs10491434 |
| geneview | rs10491434 |
| scholar | rs10491434 |
| rs10491434 | |
| pharmgkb | rs10491434 |
| gwascentral | rs10491434 |
| openSNP | rs10491434 |
| 23andMe | rs10491434 |
| SNPshot | rs10491434 |
| SNPdbe | rs10491434 |
| MSV3d | rs10491434 |
| GWAS Ctlg | rs10491434 |
| GMAF | 0.2631 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 22329520] Identification of IL7RA risk alleles for rapid progression during HIV-1 infection: a comprehensive study in the GRIV cohort
| ClinVar | |
|---|---|
| Risk | rs10491434(C;C) |
| Alt | rs10491434(C;C) |
| Reference | Rs10491434(T;T) |
| Significance | Non-pathogenic |
| Disease | Severe Combined Immune Deficiency |
| Variation | info |
| Gene | IL7R |
| CLNDBN | Severe Combined Immune Deficiency |
| Reversed | 1 |
| HGVS | NC_000005.9:g.35877914A>G |
| CLNSRC | |
| CLNACC | RCV000293662.1, |
