Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4987188
rs4987188
MSH2
0.020 GeneticVariation BEFREE Structural debilitation of mutation G322D associated with MSH2 and their role in triple negative breast cancer. 30806579

2020
dbSNP: rs4987188
rs4987188
MSH2
0.020 GeneticVariation BEFREE The Gly322Asp polymorphism of the hMSH2 gene may be linked with TNBC occurrence in Polish women. 25134804

2015