rs2236142
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2236142(C;C) |
Make rs2236142(C;G) |
Make rs2236142(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 22 |
Position | 28741956 |
Gene | CHEK2, HSCB |
is a | snp |
is | mentioned by |
dbSNP | rs2236142 |
dbSNP (classic) | rs2236142 |
ClinGen | rs2236142 |
ebi | rs2236142 |
HLI | rs2236142 |
Exac | rs2236142 |
Gnomad | rs2236142 |
Varsome | rs2236142 |
LitVar | rs2236142 |
Map | rs2236142 |
PheGenI | rs2236142 |
Biobank | rs2236142 |
1000 genomes | rs2236142 |
hgdp | rs2236142 |
ensembl | rs2236142 |
geneview | rs2236142 |
scholar | rs2236142 |
rs2236142 | |
pharmgkb | rs2236142 |
gwascentral | rs2236142 |
openSNP | rs2236142 |
23andMe | rs2236142 |
SNPshot | rs2236142 |
SNPdbe | rs2236142 |
MSV3d | rs2236142 |
GWAS Ctlg | rs2236142 |
GMAF | 0.3939 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 22201027] Variant allele of CHEK2 is associated with a decreased risk of esophageal cancer lymph node metastasis in a Chinese population
[PMID 17132159] Comprehensive analysis of the ATM, CHEK2 and ERBB2 genes in relation to breast tumour characteristics and survival: a population-based case-control and follow-up study.