CCDC33, coiled-coil domain containing 33, 80125

N. diseases: 12; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs116264669
rs116264669
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0085437
Disease:
Meningitis, Bacterial 		0.700 GeneticVariation GWASCAT Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. 31092817 2019
dbSNP: rs11638831
rs11638831
Entrez Id: 64220;80125
Gene Symbol: STRA6;CCDC33
STRA6;CCDC33
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12916871
rs12916871
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs200975846
rs200975846
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0409959
Disease:
Osteoarthritis, Knee 		T 0.700 GeneticVariation GWASCAT Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. 30664745 2019
dbSNP: rs200975846
rs200975846
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0029410
Disease:
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
dbSNP: rs900800
rs900800
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2959011
rs2959011
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs61653296
rs61653296
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0428883
Disease:
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
dbSNP: rs11635191
rs11635191
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0004096
Disease:
Asthma 		A 0.700 GeneticVariation GWASCAT Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma. 25918132 2015
dbSNP: rs9783698
rs9783698
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0162701
Disease:
Polysomnography 		A 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs2959008
rs2959008
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0006142
Disease:
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
dbSNP: rs2959008
rs2959008
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0678222
Disease:
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
dbSNP: rs2959008
rs2959008
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0678222
Disease:
Breast Carcinoma 		0.020 GeneticVariation BEFREE Two loci (rs2959008 and rs2279357) showed evidence of associations with breast cancer risk. 22606018 2012
dbSNP: rs2959008
rs2959008
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C0006142
Disease:
Malignant neoplasm of breast 		0.020 GeneticVariation BEFREE Two loci (rs2959008 and rs2279357) showed evidence of associations with breast cancer risk. 22606018 2012
dbSNP: rs903934130
rs903934130
Entrez Id: 80125
Gene Symbol: CCDC33
CCDC33
CUI: C2239176
Disease:
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