Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

Antonis C Antoniou, Karoline B Kuchenbaecker, Penny Soucy, Jonathan Beesley, Xiaoqing Chen, Lesley McGuffog, Andrew Roger Lee, Daniel Barrowdale, Sue Healey, Olga M Sinilnikova, Maria A Caligo, Niklas Loman, Katja Harbst, Annika Lindblom, Brita Arver, Richard Rosenquist, Per W. Karlsson, Kate Nathanson, Susan Domchek, Tim RebbeckAnna Jakubowska, Jan Lubinski, Katarzyna Jaworska, Katarzyna Durda, Elżbieta Złowowcka-Perłowska, Ana Osorio, Mercedes Durán, Raquel Andrés, Javier Benítez, Ute Hamann, Frans B Hogervorst, Theo A van Os, Senno Verhoef, Hanne E J Meijers-Heijboer, Juul Wijnen, Encarna B Gómez Garcia, Marjolijn J Ligtenberg, Mieke Kriege, J Margriet Collée, Margreet G E M Ausems, Jan C Oosterwijk, Susan Peock, Debra Frost, Steve D Ellis, Radka Platte, Elena Fineberg, D Gareth Evans, Thomas V Hansen, Finn C Nielsen, Anne-Marie Gerdes, CIMBA, SWE-BRCA

78 Citationer (Scopus)

Abstract

Several common alleles have been shown to be associated with breast and/or ovarian cancer risk for BRCA1 and BRCA2 mutation carriers. Recent genome-wide association studies of breast cancer have identified eight additional breast cancer susceptibility loci: rs1011970 (9p21, CDKN2A/B), rs10995190 (ZNF365), rs704010 (ZMIZ1), rs2380205 (10p15), rs614367 (11q13), rs1292011 (12q24), rs10771399 (12p11 near PTHLH) and rs865686 (9q31.2).
OriginalsprogEngelsk
TidsskriftBreast Cancer Research (Online Edition)
Vol/bind14
Udgave nummer1
Sider (fra-til)R33
ISSN1465-542X
DOI
StatusUdgivet - 2012

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