Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80357007
rs80357007
BRCA1
0.010 GeneticVariation BEFREE In a previous study, two <i>de novo</i> BRCT missense mutations of <i>BRCA1</i>, G1763V and L1786P were identified from Chinese females with familial breast cancer. 29113215

2017