Missense variants in nine genes co‐segregated with APOE ε4, including ABCA1, AKAP9, ANK3, CTSB, EED, PRDM7, SNX1, USP6NL, and WDR81 in the AD‐FBS families, while in the EFIGA families APOE ε4 segregated with missense variants in ADAMTS20, AKAP9, ANK3, CR1, SORL1, and TSPOAP1. This evidence concerns the gene ANK3 and Alzheimer disease.