Even though we did not detect a significant association between NTHL1 c.244C>T p.(Gln82Ter) and BC risk in our patient series, a much larger genotype dataset from FinnGen showed a high increased risk of BC for homozygous (OR = 44.7, P = 6.7 × 10–5) and a low increased risk for heterozygous women (OR = 1.39, P = 7.8 × 10–5). The gene discussed is NTHL1; the disease is breast cancer.