CHEK2, checkpoint kinase 2, 11200

N. diseases: 297; N. variants: 261
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17883862
rs17883862
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Another recurrent mutation with attenuated in vitro function, CHEK2-P85L, is not associated with increased breast cancer susceptibility, but exhibits a striking difference in frequency across populations with different ancestral histories. 17721994 2007
dbSNP: rs200050883
rs200050883
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The genetic variant c.1312G>T (p.D438Y) identified in a patient with a family history of breast cancer. 24390236 2014
dbSNP: rs200649225
rs200649225
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The novel CHEK2 missense variant identified in this study, R406H, is unlikely to contribute to breast cancer risk in French Canadian women. 18706089 2008
dbSNP: rs200928781
rs200928781
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE In patients without family history, Y390C carriers tend to develop breast cancer early, before 35 years of age. 25619829 2015
dbSNP: rs201206424
rs201206424
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE We also found evidence of association with breast cancer risk for three variants in CHEK2, c.349A>G OR 2.26 (95% CI 1.29 to 3.95), c.1036C>T OR 5.06 (95% CI 1.09 to 23.5) and c.538C>T OR 1.33 (95% CI 1.05 to 1.67) (p≤0.017). 27595995 2016
dbSNP: rs28909982
rs28909982
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE To evaluate the possible association of R117G and two germline variants reported elsewhere, R145W and I157T with breast cancer, we screened 737 BRCA1/2-negative familial breast cancer cases from 605 families, 459 BRCA1/2-positive cases from 335 families, and 723 controls from the United Kingdom, the Netherlands, and North America. 12610780 2003
dbSNP: rs587780170
rs587780170
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The genetic variant c.1312G>T (p.D438Y) identified in a patient with a family history of breast cancer. 24390236 2014
dbSNP: rs587780192
rs587780192
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE We also found evidence of association with breast cancer risk for three variants in CHEK2, c.349A>G OR 2.26 (95% CI 1.29 to 3.95), c.1036C>T OR 5.06 (95% CI 1.09 to 23.5) and c.538C>T OR 1.33 (95% CI 1.05 to 1.67) (p≤0.017). 27595995 2016
dbSNP: rs587782527
rs587782527
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The c.1216C>T mutation was found in a 34-year-old ovarian cancer patient from a family with two breast cancer cases. 23806170 2013
dbSNP: rs730881701
rs730881701
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE We also found evidence of association with breast cancer risk for three variants in CHEK2, c.349A>G OR 2.26 (95% CI 1.29 to 3.95), c.1036C>T OR 5.06 (95% CI 1.09 to 23.5) and c.538C>T OR 1.33 (95% CI 1.05 to 1.67) (p≤0.017). 27595995 2016
dbSNP: rs766794072
rs766794072
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE The initial two stages, which involved up to 797 high-risk BC patients, 1504 consecutive BC cases, and 1081 healthy women, indicated a potentially BC-predisposing role for 6 candidates, i.e., USP39 c.*208G > C, PZP p.Arg680Ter, LEPREL1 p.Pro636Ser, SLIT3 p.Arg154Cys, CREB3 p.Lys157Glu, and ING1 p.Pro319Leu. 31754952 2020
dbSNP: rs77130927
rs77130927
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE We also found evidence of association with breast cancer risk for three variants in CHEK2, c.349A>G OR 2.26 (95% CI 1.29 to 3.95), c.1036C>T OR 5.06 (95% CI 1.09 to 23.5) and c.538C>T OR 1.33 (95% CI 1.05 to 1.67) (p≤0.017). 27595995 2016
dbSNP: rs9620817
rs9620817
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE In addition, we found four low-frequency variants (rs8176085, rs799923, rs8176173 and rs8176258) in the BRCA1 gene, one common variant in the CHEK2 gene (rs9620817), and one common variant in the PALB2 gene (rs13330119) associated with breast cancer risk at P < 0.01. 28419251 2017
dbSNP: rs17879961
rs17879961
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
G 0.900 GeneticVariation CLINVAR
dbSNP: rs137853007
rs137853007
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
A 0.700 GeneticVariation CLINVAR
dbSNP: rs555607708
rs555607708
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
A 0.700 CausalMutation CLINVAR
dbSNP: rs587780174
rs587780174
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
T 0.700 CausalMutation CLINVAR
dbSNP: rs587782471
rs587782471
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
G 0.700 GeneticVariation CLINVAR
dbSNP: rs864622149
rs864622149
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
T 0.700 GeneticVariation CLINVAR
dbSNP: rs17879961
rs17879961
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
G 0.900 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs17879961
rs17879961
Entrez Id: 11200
Gene Symbol: CHEK2
CHEK2
CUI: C0678222
Disease:
Breast Carcinoma
G 0.900 GeneticVariation GWASCAT Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. 25751625 2015