CCND2, cyclin D2, 894

N. diseases: 241; N. variants: 15
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.800 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.800 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.800 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		0.800 GeneticVariation UNIPROT De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. 24705253 2014
dbSNP: rs587777620
rs587777620
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		0.800 GeneticVariation UNIPROT De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. 24705253 2014
dbSNP: rs587777620
rs587777620
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		A 0.800 CausalMutation CLINVAR De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. 24705253 2014
dbSNP: rs587777622
rs587777622
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		0.800 GeneticVariation UNIPROT De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. 24705253 2014
dbSNP: rs777786993
rs777786993
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		0.800 GeneticVariation UNIPROT De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. 24705253 2014
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.800 GeneticVariation GWASDB Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009402
Disease:
Colorectal Carcinoma 		T 0.800 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3217901
rs3217901
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009402
Disease:
Colorectal Carcinoma 		G 0.800 GeneticVariation GWASDB Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs3217901
rs3217901
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009402
Disease:
Colorectal Carcinoma 		G 0.800 GeneticVariation GWASCAT Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. 23266556 2013
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		G 0.800 CausalMutation CLINVAR
dbSNP: rs587777622
rs587777622
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		T 0.800 CausalMutation CLINVAR
dbSNP: rs587777622
rs587777622
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		G 0.800 CausalMutation CLINVAR
dbSNP: rs777786993
rs777786993
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C4014742
Disease:
MEGALENCEPHALY-POLYMICROGYRIA-POLYDACTYLY-HYDROCEPHALUS SYNDROME 3 		G 0.800 CausalMutation CLINVAR
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0007102
Disease:
Malignant tumor of colon 		T 0.700 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009404
Disease:
Colorectal Neoplasms 		T 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C1302401
Disease:
Adenoma of large intestine 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0009404
Disease:
Colorectal Neoplasms 		T 0.700 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C1319315
Disease:
Adenocarcinoma of large intestine 		T 0.700 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		T 0.700 GeneticVariation GWASCAT Association analyses identify 31 new risk loci for colorectal cancer susceptibility. 31089142 2019
dbSNP: rs3217810
rs3217810
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0346629
Disease:
Malignant neoplasm of large intestine 		T 0.700 GeneticVariation GWASCAT Discovery of common and rare genetic risk variants for colorectal cancer. 30510241 2019