Additional file 3: of Prevalence of pathogenic/likely pathogenic variants in the 24 cancer genes of the ACMG Secondary Findings v2.0 list in a large cancer cohort and ethnicity-matched controls

dataset

posted on 2018-12-24, 05:00 authored by Jung Kim, Wen Luo, Mingyi Wang, Talia Wegman-Ostrosky, Megan Frone, Jennifer Johnston, Michael Nickerson, Melissa Rotunno, Shengchao Li, Maria Achatz, Seth Brodie, Michael Dean, Kelvin Andrade, Fernanda Fortes, Matthew Gianferante, Payal Khincha, Mary McMaster, Lisa McReynolds, Alexander Pemov, Maisa Pinheiro, Karina Santiago, Blanche Alter, Neil Caporaso, Shahinaz Gadalla, Lynn Goldin, Mark Greene, Jennifer Loud, Xiaohong Yang, Neal Freedman, Susan Gapstur, Mia Gaudet, Donato Calista, Paola Ghiorzo, Maria Fargnoli, Eduardo Nagore, Ketty Peris, Susana Puig, Maria Landi, Belynda Hicks, Bin Zhu, Jia Liu, Joshua Sampson, Stephen Chanock, Lisa Mirabello, Lindsay Morton, Leslie Biesecker, Margaret Tucker, Sharon Savage, Alisa Goldstein, Douglas Stewart

Table S2. InterVar classification of ACMG SF v2.0 cancer genes after expert review. (XLSX 30 kb)

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Division of Cancer Epidemiology and Genetics, National Cancer Institute

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ACMG secondary findings Familial cancer exome Population study Variant classification

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