MAPT and Parkinson disease: In H114, two of the “SNPs with high read-depth” (>30X sequence coverage; Additional file 1: Table S6; (Oetting 2011)), [chr17: 41400462] and [chr17:41400511], resulted in two non-synonymous mutations in MAPT (microtubule-associated protein tau), which was associated with inheritable Parkinson’s disease (Trotta et al. 2011).