BBC3, BCL2 binding component 3, 27113

N. diseases: 157; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs45474992
rs45474992
Entrez Id: 27113
Gene Symbol: BBC3
BBC3
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs45474992
rs45474992
Entrez Id: 27113
Gene Symbol: BBC3
BBC3
CUI: C0200637
Disease:
Monocyte count procedure
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs45474992
rs45474992
Entrez Id: 27113
Gene Symbol: BBC3
BBC3
CUI: C0750880
Disease:
Monocyte count result
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2032809
rs2032809
Entrez Id: 27113
Gene Symbol: BBC3
BBC3
CUI: C2349952
Disease:
Oropharyngeal Carcinoma
0.010 GeneticVariation BEFREE We found that each individual polymorphism had only a modest impact on risk of SCCHN, particularly in oropharyngeal cancer for rs3810294 and non-oropharyngeal cancer for rs2032809. 22086558 2012
dbSNP: rs2032809
rs2032809
Entrez Id: 27113
Gene Symbol: BBC3
BBC3
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck
0.010 GeneticVariation BEFREE To examine whether the PUMA variants modify the association between HPV16 serology and risk of squamous cell carcinoma of the head and neck (SCCHN), we genotyped two polymorphisms in the PUMA promoter (rs3810294 and rs2032809) in 380 cases and 335 cancer-free controls of non-Hispanic Whites, who were frequency-matched by age (±5 yr), sex, smoking, and drinking status. 22086558 2012
dbSNP: rs2032809
rs2032809
Entrez Id: 27113
Gene Symbol: BBC3
BBC3
CUI: C0153382
Disease:
Malignant neoplasm of oropharynx
0.010 GeneticVariation BEFREE We found that each individual polymorphism had only a modest impact on risk of SCCHN, particularly in oropharyngeal cancer for rs3810294 and non-oropharyngeal cancer for rs2032809. 22086558 2012
dbSNP: rs3810294
rs3810294
Entrez Id: 27113;100422832
Gene Symbol: BBC3;MIR3191
BBC3;MIR3191
CUI: C0153382
Disease:
Malignant neoplasm of oropharynx
0.010 GeneticVariation BEFREE We found that each individual polymorphism had only a modest impact on risk of SCCHN, particularly in oropharyngeal cancer for rs3810294 and non-oropharyngeal cancer for rs2032809. 22086558 2012
dbSNP: rs3810294
rs3810294
Entrez Id: 27113;100422832
Gene Symbol: BBC3;MIR3191
BBC3;MIR3191
CUI: C2349952
Disease:
Oropharyngeal Carcinoma
0.010 GeneticVariation BEFREE We found that each individual polymorphism had only a modest impact on risk of SCCHN, particularly in oropharyngeal cancer for rs3810294 and non-oropharyngeal cancer for rs2032809. 22086558 2012
dbSNP: rs3810294
rs3810294
Entrez Id: 27113;100422832
Gene Symbol: BBC3;MIR3191
BBC3;MIR3191
CUI: C1168401
Disease:
Squamous cell carcinoma of the head and neck
0.010 GeneticVariation BEFREE To examine whether the PUMA variants modify the association between HPV16 serology and risk of squamous cell carcinoma of the head and neck (SCCHN), we genotyped two polymorphisms in the PUMA promoter (rs3810294 and rs2032809) in 380 cases and 335 cancer-free controls of non-Hispanic Whites, who were frequency-matched by age (±5 yr), sex, smoking, and drinking status. 22086558 2012