rs36228499
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs36228499(G;G) |
| Make rs36228499(G;T) |
| Make rs36228499(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 12717002 |
| Gene | CDKN1B, GPR19 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs36228499 |
| dbSNP (classic) | rs36228499 |
| ClinGen | rs36228499 |
| ebi | rs36228499 |
| HLI | rs36228499 |
| Exac | rs36228499 |
| Gnomad | rs36228499 |
| Varsome | rs36228499 |
| LitVar | rs36228499 |
| Map | rs36228499 |
| PheGenI | rs36228499 |
| Biobank | rs36228499 |
| 1000 genomes | rs36228499 |
| hgdp | rs36228499 |
| ensembl | rs36228499 |
| geneview | rs36228499 |
| scholar | rs36228499 |
| rs36228499 | |
| pharmgkb | rs36228499 |
| gwascentral | rs36228499 |
| openSNP | rs36228499 |
| 23andMe | rs36228499 |
| SNPshot | rs36228499 |
| SNPdbe | rs36228499 |
| MSV3d | rs36228499 |
| GWAS Ctlg | rs36228499 |
| GMAF | 0.3976 |
| Max Magnitude | 0 |
[PMID 20075119] Allelic variant at -79 (C>T) in CDKNIB (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels [PMID 19667240] p27kip1-838C>A single nucleotide polymorphism is associated with restenosis risk after coronary stenting and modulates p27kip1 promoter activity.
[PMID 20617153
] Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia.
[PMID 23966119] Genetic Risk Factors for Hypertrophic Scar Development
