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: rs76895963
rs76895963
Entrez Id: 894;103752584
Gene Symbol: CCND2;CCND2-AS1
CCND2;CCND2-AS1
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. 28552196 2017
dbSNP: rs1049606
rs1049606
Entrez Id: 894;103752584
Gene Symbol: CCND2;CCND2-AS1
CCND2;CCND2-AS1
CUI: C0019196
Disease:
Hepatitis C 		0.010 GeneticVariation BEFREE These included novel SNPs for hepatocarcinogenesis with HCV CCND2 rs1049606, RAD23B rs1805329, CEP164 rs573455, and GRP78rs430397 in addition to the known SNPs MDM2 rs2279744 and ALDH2 rs671. 22004425 2012
dbSNP: rs1049606
rs1049606
Entrez Id: 894;103752584
Gene Symbol: CCND2;CCND2-AS1
CCND2;CCND2-AS1
CUI: C1512409
Disease:
Hepatocarcinogenesis 		0.010 GeneticVariation BEFREE These included novel SNPs for hepatocarcinogenesis with HCV CCND2 rs1049606, RAD23B rs1805329, CEP164 rs573455, and GRP78rs430397 in addition to the known SNPs MDM2 rs2279744 and ALDH2 rs671. 22004425 2012
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0026650
Disease:
Movement Disorders 		G 0.700 GeneticVariation CLINVAR The role of intermediate progenitor cells in the evolutionary expansion of the cerebral cortex. 16766701 2006
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0432072
Disease:
Dysmorphic features 		G 0.700 GeneticVariation CLINVAR The role of intermediate progenitor cells in the evolutionary expansion of the cerebral cortex. 16766701 2006
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C1849265
Disease:
Overgrowth 		G 0.700 GeneticVariation CLINVAR The role of intermediate progenitor cells in the evolutionary expansion of the cerebral cortex. 16766701 2006
dbSNP: rs587777621
rs587777621
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0000772
Disease:
Multiple congenital anomalies 		G 0.700 CausalMutation CLINVAR The role of intermediate progenitor cells in the evolutionary expansion of the cerebral cortex. 16766701 2006
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C1849265
Disease:
Overgrowth 		G 0.700 GeneticVariation CLINVAR Somatic activation of AKT3 causes hemispheric developmental brain malformations. 22500628 2012
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0026650
Disease:
Movement Disorders 		G 0.700 GeneticVariation CLINVAR Somatic activation of AKT3 causes hemispheric developmental brain malformations. 22500628 2012
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0432072
Disease:
Dysmorphic features 		G 0.700 GeneticVariation CLINVAR Somatic activation of AKT3 causes hemispheric developmental brain malformations. 22500628 2012
dbSNP: rs587777621
rs587777621
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0000772
Disease:
Multiple congenital anomalies 		G 0.700 CausalMutation CLINVAR Somatic activation of AKT3 causes hemispheric developmental brain malformations. 22500628 2012
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0026650
Disease:
Movement Disorders 		G 0.700 GeneticVariation CLINVAR Regulation of cerebral cortex size and folding by expansion of basal progenitors. 23624932 2013
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C1849265
Disease:
Overgrowth 		G 0.700 GeneticVariation CLINVAR Regulation of cerebral cortex size and folding by expansion of basal progenitors. 23624932 2013
dbSNP: rs587777618
rs587777618
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0432072
Disease:
Dysmorphic features 		G 0.700 GeneticVariation CLINVAR Regulation of cerebral cortex size and folding by expansion of basal progenitors. 23624932 2013
dbSNP: rs587777621
rs587777621
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0000772
Disease:
Multiple congenital anomalies 		G 0.700 CausalMutation CLINVAR Regulation of cerebral cortex size and folding by expansion of basal progenitors. 23624932 2013
dbSNP: rs76895963
rs76895963
Entrez Id: 894;103752584
Gene Symbol: CCND2;CCND2-AS1
CCND2;CCND2-AS1
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		T 0.700 GeneticVariation GWASCAT Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. 29358691 2018
dbSNP: rs3217869
rs3217869
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0600139
Disease:
Prostate carcinoma 		0.010 GeneticVariation BEFREE Our functional analysis revealed a statistically significant relationship between rs3217869 risk genotype and decreased CCND2 expression levels in a collection of 119 prostate cancer patient samples. 28674394 2017
dbSNP: rs3217869
rs3217869
Entrez Id: 894
Gene Symbol: CCND2
CCND2
CUI: C0376358
Disease:
Malignant neoplasm of prostate 		0.010 GeneticVariation BEFREE Our functional analysis revealed a statistically significant relationship between rs3217869 risk genotype and decreased CCND2 expression levels in a collection of 119 prostate cancer patient samples. 28674394 2017
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: 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 Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119 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: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12 		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: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1 		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: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10 		T 0.700 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119 2019