PT - JOURNAL ARTICLE AU - Yuan Chun Ding AU - Aaron W. Adamson AU - Mehrdad Bakhtiari AU - Carmina Patrick AU - Jonghun Park AU - Yael Laitman AU - Jeffrey N. Weitzel AU - Vineet Bafna AU - Eitan Friedman AU - Susan L. Neuhausen TI - Variable Number Tandem Repeats (VNTRs) as modifiers of breast cancer risk in carriers of <em>BRCA1</em> 185delAG AID - 10.1101/2022.06.01.494371 DP - 2022 Jan 01 TA - bioRxiv PG - 2022.06.01.494371 4099 - http://biorxiv.org/content/early/2022/06/02/2022.06.01.494371.short 4100 - http://biorxiv.org/content/early/2022/06/02/2022.06.01.494371.full AB - Despite substantial efforts in identifying both rare and common variants affecting disease risk, in the majority of diseases, a large proportion of unexplained genetic risk remains. We propose that variable number tandem repeats (VNTRs) may explain a proportion of the missing genetic risk. Herein, we tested whether VNTRs are causal modifiers of breast cancer risk in 347 female carriers of BRCA1 185delAG, an important group given their high risk of developing breast cancer. We performed targeted-capture to sequence VNTRs, called genotypes with adVNTR, and tested the association of VNTRs and breast cancer risk using Cox regression models. Of 303 VNTRs that passed quality control checks, 4 VNTRs were significantly associated with risk to develop breast cancer at false discovery rate [FDR] &lt; 0.05 and an additional 4 VNTRs had FDR &lt; 0.25. After determining the specific risk alleles, there was a significantly earlier age at development of breast cancer in carriers of the risk genotypes compared to those without the risk genotypes for seven of eight VNTRs. Results from this first systematic study of VNTRs demonstrate that VNTRs may explain a proportion of the unexplained genetic risk for disease and have larger effects than SNPs.Competing Interest StatementThe authors have declared no competing interest.