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'''Table 5: Genes with known hereditary risk associations in breast cancer according to National Comprehensive Cancer Network (NCCN) Guidelines (version 3.2019)'''
{| class="wikitable"
|'''Gene'''
|'''Associated Syndrome; Breast Cancer Subtype'''
|-
|''ATM''
|Ataxia telangiectasia syndrome
|-
|''BRCA1''
|BRCA-Related Breast/ Ovarian Cancer Syndrome; TNBC
|-
|''BRCA2''
|BRCA-Related Breast/ Ovarian Cancer Syndrome; TNBC
|-
|''CDH1''
|Hereditary Diffuse Gastric Cancer and Lobular Breast Cancer
|-
|''CHEK2''
|Inherited breast cancer
|-
|''NBN''
|Nijmegen Breakage Syndrome (autosomal recessive inheritance)
|-
|''NF1''
|Neurofibromatosis type 1
|-
|''PALB2''
|Fanconi anemia
|-
|''PTEN''
|Cowden syndrome
|-
|''STK11''
|Peutz-Jeghers syndrome
|-
|''TP53''
|Li-Fraumeni syndrome
|}
Inheritance is autosomal dominant with incomplete penetrance, unless otherwise specified
'''General Disease Overview / Description of Cancer Category'''
'''General Disease Overview / Description of Cancer Category'''