rs2236141
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs2236141(C;C) |
| Make rs2236141(C;T) |
| Make rs2236141(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 28741882 |
| Gene | CHEK2, HSCB |
| is a | snp |
| is | mentioned by |
| dbSNP | rs2236141 |
| dbSNP (classic) | rs2236141 |
| ClinGen | rs2236141 |
| ebi | rs2236141 |
| HLI | rs2236141 |
| Exac | rs2236141 |
| Gnomad | rs2236141 |
| Varsome | rs2236141 |
| LitVar | rs2236141 |
| Map | rs2236141 |
| PheGenI | rs2236141 |
| Biobank | rs2236141 |
| 1000 genomes | rs2236141 |
| hgdp | rs2236141 |
| ensembl | rs2236141 |
| geneview | rs2236141 |
| scholar | rs2236141 |
| rs2236141 | |
| pharmgkb | rs2236141 |
| gwascentral | rs2236141 |
| openSNP | rs2236141 |
| 23andMe | rs2236141 |
| SNPshot | rs2236141 |
| SNPdbe | rs2236141 |
| MSV3d | rs2236141 |
| GWAS Ctlg | rs2236141 |
| GMAF | 0.107 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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| ||
[PMID 20462940] A variant in the CHEK2 promoter at a methylation site relieves transcriptional repression and confers reduced risk of lung cancer
[PMID 22201027] Variant allele of CHEK2 is associated with a decreased risk of esophageal cancer lymph node metastasis in a Chinese population
[PMID 17428325
] Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.
