Variant: rs1060502716

present in Gene: CHEK2 present in Chromosome: 22 Position on Chromosome: 28695874 Alleles of this Variant: C/A;G;T

rs1060502716 in CHEK2 gene and Malignant neoplasm of breast PMID 21876083 2011 Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer.

PMID 24713400 2014 A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central Poland.

rs1060502716 in CHEK2 gene and Multiple congenital anomalies PMID 22058428 2011 CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women.

PMID 25467110 2015 Beyond BRCA: new hereditary breast cancer susceptibility genes.

PMID 26506619 2015 Association of Germline CHEK2 Gene Variants with Risk and Prognosis of Non-Hodgkin Lymphoma.

PMID 15122511 2004 CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies.

PMID 11719428 2001 Destabilization of CHK2 by a missense mutation associated with Li-Fraumeni Syndrome.

PMID 23296741 2013 The risk of gastric cancer in carriers of CHEK2 mutations.

PMID 18004398 2007 CHK2 kinase: cancer susceptibility and cancer therapy - two sides of the same coin?

PMID 19338683 2009 The contribution of CHEK2 to the TP53-negative Li-Fraumeni phenotype.

PMID 18759107 2009 CHEK2 1100delC and male breast cancer in the Netherlands.

PMID 16551709 2006 Spectrum of mutations in BRCA1, BRCA2, CHEK2, and TP53 in families at high risk of breast cancer.

PMID 15492928 2004 CHEK2 is a multiorgan cancer susceptibility gene.

PMID 16078115 2005 CHEK2 mutations in primary glioblastomas.

PMID 21807500 2011 Meta-analysis of CHEK2 1100delC variant and colorectal cancer susceptibility.

PMID 21876083 2011 Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer.