rs35211496
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs35211496(C;T) |
| Make rs35211496(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 18 |
| Position | 62354528 |
| Gene | TNFRSF11A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs35211496 |
| dbSNP (classic) | rs35211496 |
| ClinGen | rs35211496 |
| ebi | rs35211496 |
| HLI | rs35211496 |
| Exac | rs35211496 |
| Gnomad | rs35211496 |
| Varsome | rs35211496 |
| LitVar | rs35211496 |
| Map | rs35211496 |
| PheGenI | rs35211496 |
| Biobank | rs35211496 |
| 1000 genomes | rs35211496 |
| hgdp | rs35211496 |
| ensembl | rs35211496 |
| geneview | rs35211496 |
| scholar | rs35211496 |
| rs35211496 | |
| pharmgkb | rs35211496 |
| gwascentral | rs35211496 |
| openSNP | rs35211496 |
| 23andMe | rs35211496 |
| SNPshot | rs35211496 |
| SNPdbe | rs35211496 |
| MSV3d | rs35211496 |
| GWAS Ctlg | rs35211496 |
| GMAF | 0.08035 |
| Max Magnitude | 0 |
[PMID 20231205] Genetic Variations in Genes Encoding RANK, RANKL, and OPG in Rheumatoid Arthritis: A Case-Control Study
[PMID 20564239] Genetic variation in the TNFRSF11A gene encoding RANK is associated with susceptibility to Paget's disease of bone
[PMID 23369128
] Genetic polymorphism of the OPG gene associated with breast cancer
[PMID 24921058] Receptor activator of nuclear factor kappa-B gene polymorphisms in Iranian periodontitis and peri-implantitis patients
| ClinVar | |
|---|---|
| Risk | rs35211496(T;T) |
| Alt | rs35211496(T;T) |
| Reference | Rs35211496(C;C) |
| Significance | Probable-non-pathogenic |
| Disease | Paget disease of bone Osteopetrosis not specified |
| Variation | info |
| Gene | TNFRSF11A |
| CLNDBN | Paget disease of bone Osteopetrosis not specified |
| Reversed | 0 |
| HGVS | NC_000018.9:g.60021761C>T |
| CLNSRC | |
| CLNACC | RCV000269060.1, RCV000363657.1, RCV000454965.1, |
