Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4986764
rs4986764
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0678222
Disease:
Breast Carcinoma
0.040 GeneticVariation BEFREE The results showed a decreased risk of rs2048718 or rs4986764 for cervical cancer rather than breast cancer in the overall population (<i>P</i> < 0.05). 29466248 2018
dbSNP: rs4986764
rs4986764
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0678222
Disease:
Breast Carcinoma
0.040 GeneticVariation BEFREE Accordingly, C47G and G64A polymorphisms were studied in 1,539 cases and 1,183 controls, and 667 and 782, respectively.In the overall analysis, association was lacking between the Pro919Ser polymorphism and breast cancer risk (odds ratio [OR] 0.98-1.02), materially unchanged when confined to subjects of European ancestry (OR 0.96-1.03) or even in the high-powered studies (OR 0.97-1.03). 23225146 2013
dbSNP: rs4986764
rs4986764
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0678222
Disease:
Breast Carcinoma
0.040 GeneticVariation BEFREE We found no effect of the putatively functional BRIP1 variants -64G>A and Pro919Ser on the risk of familial BC. 17504528 2007
dbSNP: rs4986764
rs4986764
Entrez Id: 83990
Gene Symbol: BRIP1
BRIP1
CUI: C0678222
Disease:
Breast Carcinoma
0.040 GeneticVariation BEFREE Recently, one of the observed common variants, Ser-allele of the Ser919Pro polymorphism, was suggested to associate with an increased breast cancer risk, and was here evaluated in an independent, large series of 888 unselected breast cancer patients and in 736 healthy controls. 16430786 2006