CCND1, cyclin D1, 595

N. diseases: 859; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C1858438
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO
A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C3805838
Disease:
VON HIPPEL-LINDAU SYNDROME, MODIFIER OF
A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C3810481
Disease:
MULTIPLE MYELOMA, t(11;14) TYPE, SUSCEPTIBILITY TO
A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs603965
rs603965
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin
0.010 GeneticVariation BEFREE The cyclin D1 (CCND1) splice variant G870A (rs603965) increased NHL risk (OR(AA) = 1.4, 95% CI = 1.1-1.8, P-trend = 0.021), which was consistent for four B-cell subtypes. 16783567 2006
dbSNP: rs766170770
rs766170770
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE The findings of this pilot study suggest that the cyclin D1 A870G and the EGF A61G polymorphisms may be useful molecular markers for predicting clinical outcome in CRC patients treated with single-agent Cetuximab. 16788380 2006
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C4048328
Disease:
cervical cancer
0.040 GeneticVariation BEFREE A significant association of CxCa with various polymorphisms was observed: rs1800797 in the IL-6 gene (odds ratio [OR] = 0.88, 95% confidence intervals [CI]: 0.79-0.99); rs1041981 in the LTA gene (OR = 0.87, 95% CI: 0.78-0.98), and rs9344 in the CCND1 gene (OR = 1.14, 95% CI: 1.02-1.27), for those individuals carrying the rare allele. 19585495 2009
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0007847
Disease:
Malignant tumor of cervix
0.040 GeneticVariation BEFREE A significant association of CxCa with various polymorphisms was observed: rs1800797 in the IL-6 gene (odds ratio [OR] = 0.88, 95% confidence intervals [CI]: 0.79-0.99); rs1041981 in the LTA gene (OR = 0.87, 95% CI: 0.78-0.98), and rs9344 in the CCND1 gene (OR = 1.14, 95% CI: 1.02-1.27), for those individuals carrying the rare allele. 19585495 2009
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0302592
Disease:
Cervix carcinoma
0.040 GeneticVariation BEFREE A significant association of CxCa with various polymorphisms was observed: rs1800797 in the IL-6 gene (odds ratio [OR] = 0.88, 95% confidence intervals [CI]: 0.79-0.99); rs1041981 in the LTA gene (OR = 0.87, 95% CI: 0.78-0.98), and rs9344 in the CCND1 gene (OR = 1.14, 95% CI: 1.02-1.27), for those individuals carrying the rare allele. 19585495 2009
dbSNP: rs3212879
rs3212879
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE The most significant association of CCND1 SNP rs3212879 with estrogen receptor-negative tumor types (P = 0.001) did not reach genome-wide significance levels. 19124506 2009
dbSNP: rs766170770
rs766170770
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C1167791
Disease:
Skin toxicity
0.010 GeneticVariation BEFREE Associations of epidermal growth factor (EGF) 61A>G, EGF receptor (EGFR) CA(14-22), cyclin D1 (CCND1) 932G>A, fragment-C gamma receptor (FCGR) 2A 535A>G and FCGR3A 818A>C polymorphisms with progression-free survival (PFS) and cetuximab-related skin toxicity were studied. 20418097 2010
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0678222
Disease:
Breast Carcinoma
0.010 GeneticVariation BEFREE Four single nucleotide polymorphisms (SNPs) in three genes were genotyped by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry [CCND1 Ex4-1G>A (rs9344), CDK7 Ex2-28C>T (rs2972388), ESR1 P325P Ex4-122G>C (rs1801132), and ESR1 T594T Ex8+229G>A (rs2228480)], and their associations with breast cancer risk were assessed. 19941161 2010
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.010 GeneticVariation BEFREE Four single nucleotide polymorphisms (SNPs) in three genes were genotyped by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry [CCND1 Ex4-1G>A (rs9344), CDK7 Ex2-28C>T (rs2972388), ESR1 P325P Ex4-122G>C (rs1801132), and ESR1 T594T Ex8+229G>A (rs2228480)], and their associations with breast cancer risk were assessed. 19941161 2010
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0302592
Disease:
Cervix carcinoma
0.040 GeneticVariation BEFREE We examined the distribution of the CCND1 A870G (rs9344) polymorphic variant in patients with cervical cancer (n = 129) and healthy individuals (n = 288) in a sample of a Polish cohort. 20680537 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C4048328
Disease:
cervical cancer
0.040 GeneticVariation BEFREE We examined the distribution of the CCND1 A870G (rs9344) polymorphic variant in patients with cervical cancer (n = 129) and healthy individuals (n = 288) in a sample of a Polish cohort. 20680537 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0007847
Disease:
Malignant tumor of cervix
0.040 GeneticVariation BEFREE We examined the distribution of the CCND1 A870G (rs9344) polymorphic variant in patients with cervical cancer (n = 129) and healthy individuals (n = 288) in a sample of a Polish cohort. 20680537 2011
dbSNP: rs678653
rs678653
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus
0.010 GeneticVariation BEFREE Investigation of potential association of SNPs (G870A, rs9344; G1722C, rs678653) of cyclin D1 gene (CCND1) with susceptibility to esophageal squamous cell carcinoma (ESCC) in Kashmir valley (India). 21268129 2011
dbSNP: rs678653
rs678653
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0220641
Disease:
Lip and Oral Cavity Carcinoma
0.010 GeneticVariation BEFREE This study aimed to investigate the association of CCND1 single nucleotide polymorphisms A870G (rs9344) and C1722G (rs678653) with oral cancer risk and examine the interaction between CCND1 and smoking habit. 21273603 2011
dbSNP: rs678653
rs678653
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0153381
Disease:
Malignant neoplasm of mouth
0.010 GeneticVariation BEFREE This study aimed to investigate the association of CCND1 single nucleotide polymorphisms A870G (rs9344) and C1722G (rs678653) with oral cancer risk and examine the interaction between CCND1 and smoking habit. 21273603 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0242379
Disease:
Malignant neoplasm of lung
0.010 GeneticVariation BEFREE These findings support the conclusion that cell cycle regulation may play a role in lung cancer development and that CCND1 rs9344 polymorphism together with smoking habit maybe a useful biomarker for lung cancer prediction. 21965784 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0220641
Disease:
Lip and Oral Cavity Carcinoma
0.010 GeneticVariation BEFREE Significant differences were shown between the or</span>al cancer and control groups in the distribution of the genotypes (p=0.0014) and allelic frequency (p=0.0027) in the CCND1 rs9344 genotype. 21273603 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE These findings support the conclusion that cell cycle regulation may play a role in lung cancer development and that CCND1 rs9344 polymorphism together with smoking habit maybe a useful biomarker for lung cancer prediction. 21965784 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE These findings support the conclusion that cell cycle regulation may play a role in lung cancer development and that CCND1 rs9344 polymorphism together with smoking habit maybe a useful biomarker for lung cancer prediction. 21965784 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0596263
Disease:
Carcinogenesis
0.010 GeneticVariation BEFREE Cell cycle regulation may play a role in oral carcinogenesis and CCND1 rs9344 polymorphism maybe a useful biomarker for oral oncology. 21273603 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C0153381
Disease:
Malignant neoplasm of mouth
0.010 GeneticVariation BEFREE Significant differences were shown between the or</span>al cancer and control groups in the distribution of the genotypes (p=0.0014) and allelic frequency (p=0.0027) in the CCND1 rs9344 genotype. 21273603 2011
dbSNP: rs9344
rs9344
Entrez Id: 595
Gene Symbol: CCND1
CCND1
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck
0.010 GeneticVariation BEFREE By grouping patients according to stage and radiation treatment, we compared SCCHN survival with regard to ERCC2 A35931C (Lys751Gln, rs13181) and CCND1 G870A (Pro241Pro, rs9344) genotypes. 21890746 2011