rs1049606
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1049606(C;C) |
| Make rs1049606(C;T) |
| Make rs1049606(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 4273870 |
| Gene | CCND2, CCND2-AS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1049606 |
| dbSNP (classic) | rs1049606 |
| ClinGen | rs1049606 |
| ebi | rs1049606 |
| HLI | rs1049606 |
| Exac | rs1049606 |
| Gnomad | rs1049606 |
| Varsome | rs1049606 |
| LitVar | rs1049606 |
| Map | rs1049606 |
| PheGenI | rs1049606 |
| Biobank | rs1049606 |
| 1000 genomes | rs1049606 |
| hgdp | rs1049606 |
| ensembl | rs1049606 |
| geneview | rs1049606 |
| scholar | rs1049606 |
| rs1049606 | |
| pharmgkb | rs1049606 |
| gwascentral | rs1049606 |
| openSNP | rs1049606 |
| 23andMe | rs1049606 |
| SNPshot | rs1049606 |
| SNPdbe | rs1049606 |
| MSV3d | rs1049606 |
| GWAS Ctlg | rs1049606 |
| GMAF | 0.3838 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 20414251] CCND2 polymorphisms associated with clearance of HBV Infection
[PMID 17267408
] Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms in cancer cells.
[PMID 19258477] Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.
[PMID 22004425] Genetic risk of hepatocellular carcinoma in patients with hepatitis C virus: a case control study.
