rs7958311
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7958311(A;A) |
| Make rs7958311(A;G) |
| Make rs7958311(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 121167552 |
| Gene | LOC105370032, P2RX7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7958311 |
| dbSNP (classic) | rs7958311 |
| ClinGen | rs7958311 |
| ebi | rs7958311 |
| HLI | rs7958311 |
| Exac | rs7958311 |
| Gnomad | rs7958311 |
| Varsome | rs7958311 |
| LitVar | rs7958311 |
| Map | rs7958311 |
| PheGenI | rs7958311 |
| Biobank | rs7958311 |
| 1000 genomes | rs7958311 |
| hgdp | rs7958311 |
| ensembl | rs7958311 |
| geneview | rs7958311 |
| scholar | rs7958311 |
| rs7958311 | |
| pharmgkb | rs7958311 |
| gwascentral | rs7958311 |
| openSNP | rs7958311 |
| 23andMe | rs7958311 |
| SNPshot | rs7958311 |
| SNPdbe | rs7958311 |
| MSV3d | rs7958311 |
| GWAS Ctlg | rs7958311 |
| GMAF | 0.2893 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
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[PMID 22447075
] Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity
[PMID 19319666] Genetics of the P2X7 receptor and human disease.
[PMID 19838818] Identification and characterization of a novel variant of the human P2X(7) receptor resulting in gain of function.
[PMID 27672203] P2X7R Gene Polymorphisms Are Associated with Increased Risk of Pulmonary Tuberculosis in the Tibetan Chinese Population.
[PMID 28495473] Genetic polymorphisms of the P2X7 gene associated with susceptibility to and prognosis of pulmonary tuberculosis.
[PMID 30992418] Genetic variation of rs7958311 in P2X7R gene is associated with the susceptibility and disease activity of ankylosing spondylitis.
