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rs2236141

From SNPedia

Orientationplus
Stabilizedplus
Make rs2236141(C;C)
Make rs2236141(C;T)
Make rs2236141(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position28741882
GeneCHEK2, HSCB
is asnp
is mentioned by
dbSNPrs2236141
ebirs2236141
HLIrs2236141
Exacrs2236141
Varsomers2236141
Maprs2236141
PheGenIrs2236141
hapmaprs2236141
1000 genomesrs2236141
hgdprs2236141
ensemblrs2236141
gopubmedrs2236141
geneviewrs2236141
scholarrs2236141
googlers2236141
pharmgkbrs2236141
gwascentralrs2236141
openSNPrs2236141
23andMers2236141
23andMe allrs2236141
SNP Nexus

SNPshotrs2236141
SNPdbers2236141
MSV3drs2236141
GWAS Ctlgrs2236141
GMAF0.107
Max Magnitude
? (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 17428325OA-icon.png] Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk.