The variant with the highest CADD score was rs17651549 (Pmtag = 1.69 × 10−24, CADD score 26.8) in 17q21.31 locus, which is an exonic variant of MAPT. RegulomeDB scores showed that the variant rs17572495 (Pmtag = 1.36 × 10−23) had a relatively higher regulation level, which was also in the 17q21.31 locus located in the 5′UTR of MAPT. Note that both rs17651549 and rs17572495 were verified to be in the optimal subset of trait {LBD, PD} from the ASSET analysis, which further highlighted the role of MAPT in the shared genetic etiology of LBD and PD. The gene discussed is MAPT; the disease is Parkinson disease.