rs10204525
| Orientation | minus |
| Stabilized | minus |
| Make rs10204525(A;A) |
| Make rs10204525(A;G) |
| Make rs10204525(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 241850169 |
| Gene | PDCD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10204525 |
| dbSNP (classic) | rs10204525 |
| ClinGen | rs10204525 |
| ebi | rs10204525 |
| HLI | rs10204525 |
| Exac | rs10204525 |
| Gnomad | rs10204525 |
| Varsome | rs10204525 |
| LitVar | rs10204525 |
| Map | rs10204525 |
| PheGenI | rs10204525 |
| Biobank | rs10204525 |
| 1000 genomes | rs10204525 |
| hgdp | rs10204525 |
| ensembl | rs10204525 |
| geneview | rs10204525 |
| scholar | rs10204525 |
| rs10204525 | |
| pharmgkb | rs10204525 |
| gwascentral | rs10204525 |
| openSNP | rs10204525 |
| 23andMe | rs10204525 |
| SNPshot | rs10204525 |
| SNPdbe | rs10204525 |
| MSV3d | rs10204525 |
| GWAS Ctlg | rs10204525 |
| GMAF | 0.3728 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 23373967] Association between polymorphisms in PDCD1 gene and aplastic anemia in Chinese Han population
[PMID 24389076] Programmed Death-1 (PD-1) Polymorphisms in Chinese patients with esophageal cancer
[PMID 19234630
] PDCD1 genes may protect against extraocular manifestations in Chinese Han patients with Vogt-Koyanagi-Harada syndrome.
[PMID 25218665] PD-1 mRNA expression is associated with clinical and viral profile and PD1 3'-untranslated region polymorphism in patients with chronic HBV infection
[PMID 25747035] Genetic variations of IL-28B and PD-1 are in association with the susceptibility and outcomes of HCV infection in Southeast China
[PMID 27751353] Association of programmed death-1 polymorphisms with the risk and prognosis of esophageal squamous cell carcinoma.
[PMID 29774466] Rs2227982 and rs2227981 in PDCD1 gene are functional SNPs associated with T1D risk in East Asian.
[PMID 30594267] Association of a PD-L2 Gene Polymorphism with Chronic Lymphatic Filariasis in a South Indian Cohort.
[PMID 31464942] Association of rs10204525 genotype GG and rs2227982 CC combination in programmed cell death 1 with hepatitis B virus infection risk.
[PMID 33255938] SNP-SNP Interaction in Genes Encoding PD-1/PD-L1 Axis as a Potential Risk Factor for Clear Cell Renal Cell Carcinoma.
