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 |
---|---|---|
|
[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.