rs35933842
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs35933842(A;A) |
| Make rs35933842(A;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 121133096 |
| Gene | LOC105370032, P2RX7 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35933842 |
| dbSNP (classic) | rs35933842 |
| ClinGen | rs35933842 |
| ebi | rs35933842 |
| HLI | rs35933842 |
| Exac | rs35933842 |
| Gnomad | rs35933842 |
| Varsome | rs35933842 |
| LitVar | rs35933842 |
| Map | rs35933842 |
| PheGenI | rs35933842 |
| Biobank | rs35933842 |
| 1000 genomes | rs35933842 |
| hgdp | rs35933842 |
| ensembl | rs35933842 |
| geneview | rs35933842 |
| scholar | rs35933842 |
| rs35933842 | |
| pharmgkb | rs35933842 |
| gwascentral | rs35933842 |
| openSNP | rs35933842 |
| 23andMe | rs35933842 |
| SNPshot | rs35933842 |
| SNPdbe | rs35933842 |
| MSV3d | rs35933842 |
| GWAS Ctlg | rs35933842 |
| GMAF | 0.00551 |
| Max Magnitude | 0 |
[PMID 19891999] Functional variants of the P2RX7 gene, aseptic osteolysis, and revision of the total hip arthroplasty: a preliminary study
[PMID 22776862
] Association of P2X7 receptor polymorphisms with bone mineral density and osteoporosis risk in a cohort of Dutch fracture patients.
