rs903934130
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Liver carcinoma
0.010
GeneticVariation
BEFREE
Patients with cirrhosis complicated by HCC possessed more frequently the Leu10Pro T/ * genotype than patients without HCC (TT 20/54, CT 26/54, CC 8/54 vs TT 31/134, CT 69/134, CC 34/134; p<0.05).
18809335
2008
rs2959008
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Breast Carcinoma
0.020
GeneticVariation
BEFREE
Two loci (rs2959008 and rs2279357) showed evidence of associations with breast cancer risk.
22606018
2012
rs2959008
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Malignant neoplasm of breast
0.020
GeneticVariation
BEFREE
Two loci (rs2959008 and rs2279357) showed evidence of associations with breast cancer risk.
22606018
2012
rs9783698
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Polysomnography
A
0.700
GeneticVariation
GWASDB
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
23251661
2012
rs11635191
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Asthma
A
0.700
GeneticVariation
GWASCAT
Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma.
25918132
2015
rs2959008
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Malignant neoplasm of breast
0.020
GeneticVariation
BEFREE
Among the results for 57 SNPs and 2 gene deletions, rs1056827 in CYP1B1, rs2959008 and rs7173655 in CYP11A1, the GSTT1 gene deletion, and rs1052133 in hOGG1 showed a statistically significant interaction with acrylamide intake for ER+ breast cancer risk.
29445914
2019
rs2959008
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Breast Carcinoma
0.020
GeneticVariation
BEFREE
Among the results for 57 SNPs and 2 gene deletions, rs1056827 in CYP1B1, rs2959008 and rs7173655 in CYP11A1, the GSTT1 gene deletion, and rs1052133 in hOGG1 showed a statistically significant interaction with acrylamide intake for ER+ breast cancer risk.
29445914
2019
rs2959011
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Blood Protein Measurement
T
0.700
GeneticVariation
GWASCAT
Genomic atlas of the human plasma proteome.
29875488
2018
rs61653296
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Diastolic blood pressure
A
0.700
GeneticVariation
GWASCAT
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.
30224653
2018
rs12916871
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Systolic Pressure
A
0.700
GeneticVariation
GWASCAT
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
30578418
2019
rs11638831
STRA6;CCDC33
Body Height
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs900800
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Finding of Mean Corpuscular Hemoglobin
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs200975846
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Osteoarthritis, Knee
T
0.700
GeneticVariation
GWASCAT
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data.
30664745
2019
rs200975846
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Osteoarthritis of hip
T
0.700
GeneticVariation
GWASCAT
Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data.
30664745
2019
rs116264669
×
Entrez Id:
80125
Gene Symbol:
CCDC33
CCDC33
Meningitis, Bacterial
0.700
GeneticVariation
GWASCAT
Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis.
31092817
2019