MUTATIONS MAPT 44067400 GRCh37/hg19 rs10445337 T C Exon 6 Point, Missense Coding Unknown. Not applicable. S447P Frontotemporal Dementia: BenignNone This variant has been reported in controls and is thought to be benign (Poorkaj et al., 1998). The polymorphism resid
MUTATIONS MAPT 44067382 GRCh37/hg19 rs2258689 C T Exon 6 Point, Missense Coding Unknown. Not applicable. Y441H Frontotemporal Dementia: BenignNone This variant has been reported in healthy controls and is thought to be benign (Poorkaj et al., 1998). The polymorphis
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