Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799944
rs1799944
BRCA2
0.020 GeneticVariation BEFREE Unconditional logistic regression showed no association between rs1799943 or rs1799944 and cancer risk. 26979245

2016
dbSNP: rs1799944
rs1799944
BRCA2
0.020 GeneticVariation BEFREE We genotyped 630 unselected MM patients and over 3700 controls (newborns, age- and sex-matched healthy adults with negative cancer family histories, and the adults selected at random by family doctors) for the prevalence of three common variants of the BRCA2 (T1915M, N991D and N372H) and four common variants of the CHEK2 (1100delC, VS2+1G --> A, I157T and del5395). 18024013

2008