Among the 24 genes associated with ANM, seven genes (MSH6, TLK1, SYCP2L, BRCA1, PGAP3, DIDO1, and DDX17) were previously annotated to be responsible for the association based on distance, biological function, eQTL effect and non-synonymous SNP in high LD. The gene discussed is BRCA1; the disease is nemaline myopathy 5.