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Paper Details

Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers.
Hum Mol Genet
50
2010
), wherea, 350 SNPs, BRCA1, BRCA2, BRCA2 mutation, CAMK1D, FBXL7, LOC134997, SNPs, SNRPB, alleles o, breast cancer, candidate SNPs, rs12652447, rs6138178, rs6602595, rs9393597, single nucleotide polymorphisms

Datasets

Release 1.2