rs2069391
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2069391(C;C) |
| Make rs2069391(C;T) |
| Make rs2069391(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 55966094 |
| Gene | CDK2, PMEL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2069391 |
| dbSNP (classic) | rs2069391 |
| ClinGen | rs2069391 |
| ebi | rs2069391 |
| HLI | rs2069391 |
| Exac | rs2069391 |
| Gnomad | rs2069391 |
| Varsome | rs2069391 |
| LitVar | rs2069391 |
| Map | rs2069391 |
| PheGenI | rs2069391 |
| Biobank | rs2069391 |
| 1000 genomes | rs2069391 |
| hgdp | rs2069391 |
| ensembl | rs2069391 |
| geneview | rs2069391 |
| scholar | rs2069391 |
| rs2069391 | |
| pharmgkb | rs2069391 |
| gwascentral | rs2069391 |
| openSNP | rs2069391 |
| 23andMe | rs2069391 |
| SNPshot | rs2069391 |
| SNPdbe | rs2069391 |
| MSV3d | rs2069391 |
| GWAS Ctlg | rs2069391 |
| GMAF | 0.03994 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 19258477
] Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.
[PMID 18778477] Genomic variation in myeloma: design, content, and initial application of the Bank On A Cure SNP Panel to detect associations with progression-free survival.
