{{Rsnum
|rsid=121908701
|Chromosome=22
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CHEK2
|position=28725027
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHEK2
}}{{omim
|id=604373
|rsnum=121908701
|variant=0009
}}{{ClinVar
|rsid=121908701
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=29121015
|CHROM=22
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=CHEK2:11200
|GENE_NAME=CHEK2
|GENE_ID=11200
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000022.10:g.29121015C>T
|CLNORIGIN=1
|CLNSIG=255
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000005946.2
|CLNDBN=Prostate cancer, somatic
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=604373.0009
|Disease=Prostate cancer
}}{{PMID Auto
|PMID=12533788
|Title=Mutations in CHEK2 associated with prostate cancer risk.
|OA=1
}}

{{PMID Auto
|PMID=15095295
|Title=Limited relevance of the CHEK2 gene in hereditary breast cancer.
}}