rs2305619
| Orientation | plus |
| Stabilized | plus |
| Make rs2305619(A;A) |
| Make rs2305619(A;G) |
| Make rs2305619(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 157437072 |
| Gene | PTX3, VEPH1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2305619 |
| dbSNP (classic) | rs2305619 |
| ClinGen | rs2305619 |
| ebi | rs2305619 |
| HLI | rs2305619 |
| Exac | rs2305619 |
| Gnomad | rs2305619 |
| Varsome | rs2305619 |
| LitVar | rs2305619 |
| Map | rs2305619 |
| PheGenI | rs2305619 |
| Biobank | rs2305619 |
| 1000 genomes | rs2305619 |
| hgdp | rs2305619 |
| ensembl | rs2305619 |
| geneview | rs2305619 |
| scholar | rs2305619 |
| rs2305619 | |
| pharmgkb | rs2305619 |
| gwascentral | rs2305619 |
| openSNP | rs2305619 |
| 23andMe | rs2305619 |
| SNPshot | rs2305619 |
| SNPdbe | rs2305619 |
| MSV3d | rs2305619 |
| GWAS Ctlg | rs2305619 |
| GMAF | 0.4509 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 22822025
] Variation in PTX3 is Associated With Primary Graft Dysfunction After Lung Transplantation
[PMID 19503741] Coding variant Met72Thr in the PEDF gene and risk of neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
[PMID 19753309] SOD2 gene polymorphisms in neovascular age-related macular degeneration and polypoidal choroidal vasculopathy.
[PMID 20157514] Positive association of common variants in CD36 with neovascular age-related macular degeneration.
[PMID 23285251] Influence of pentraxin 3 (PTX3) genetic variants on myocardial infarction risk and PTX3 plasma levels
[PMID 26400151] Genetic variation in PTX3 and plasma levels associated with hepatocellular carcinoma in patients with HCV
[PMID 29020397] Pentraxin 3 gene polymorphisms and pulmonary aspergillosis in COPD patients.
[PMID 33240991] Pentraxin-3 polymorphisms and pulmonary fungal disease in non-neutropenic patients.
[PMID 33320373] PTX3 gene polymorphism associated with cryptococcosis in HIV-uninfected Chinese patients.
