rs13706
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 2 | Decreased risk for certain cancers |
| (G;G) | 0 | common in complete genomics |
| Make rs13706(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 40300899 |
| Gene | CDC6 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs13706 |
| dbSNP (classic) | rs13706 |
| ClinGen | rs13706 |
| ebi | rs13706 |
| HLI | rs13706 |
| Exac | rs13706 |
| Gnomad | rs13706 |
| Varsome | rs13706 |
| LitVar | rs13706 |
| Map | rs13706 |
| PheGenI | rs13706 |
| Biobank | rs13706 |
| 1000 genomes | rs13706 |
| hgdp | rs13706 |
| ensembl | rs13706 |
| geneview | rs13706 |
| scholar | rs13706 |
| rs13706 | |
| pharmgkb | rs13706 |
| gwascentral | rs13706 |
| openSNP | rs13706 |
| 23andMe | rs13706 |
| SNPshot | rs13706 |
| SNPdbe | rs13706 |
| MSV3d | rs13706 |
| GWAS Ctlg | rs13706 |
| GMAF | 0.2782 |
| Max Magnitude | 2 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 19233139] A novel polymorphism in CDC6 is associated with the decline in lung function of ex-smokers in COPD.
[PMID 20606534] Association Between the CDC6 G1321A Polymorphism and the Risk of Cervical Cancer
[PMID 19101572] Association analysis between the Cdc6 G1321A polymorphism and the risk for non-Hodgkin lymphoma and hepatocellular carcinoma.
| ClinVar | |
|---|---|
| Risk | Rs13706(A;A) rs13706(C;C) |
| Alt | Rs13706(A;A) rs13706(C;C) |
| Reference | Rs13706(G;G) |
| Significance | Other |
| Disease | not specified Meier-Gorlin syndrome |
| Variation | info |
| Gene | CDC6 |
| CLNDBN | not specified Meier-Gorlin syndrome |
| Reversed | 0 |
| HGVS | NC_000017.10:g.38457151G>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000116607.3, RCV000365723.1, |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 17
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d
