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rs2236142

From SNPedia

Orientationplus
Stabilizedplus
Make rs2236142(C;C)
Make rs2236142(C;G)
Make rs2236142(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position28741956
GeneCHEK2, HSCB
is asnp
is mentioned by
dbSNPrs2236142
ebirs2236142
HLIrs2236142
Exacrs2236142
Varsomers2236142
Maprs2236142
PheGenIrs2236142
hapmaprs2236142
1000 genomesrs2236142
hgdprs2236142
ensemblrs2236142
gopubmedrs2236142
geneviewrs2236142
scholarrs2236142
googlers2236142
pharmgkbrs2236142
gwascentralrs2236142
openSNPrs2236142
23andMers2236142
23andMe allrs2236142
SNP Nexus

SNPshotrs2236142
SNPdbers2236142
MSV3drs2236142
GWAS Ctlgrs2236142
GMAF0.3939
Max Magnitude
? (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 17132159OA-icon.png] 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.