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MAPT A227A

MUTATIONS MAPT 44073889 GRCh37/hg19 rs1052553 A G g.109929A> G g.107103A> G Exon 9 Point, Silent Coding Unknown. This variant segregates with the H2 haplotype, which may be associated with decreased tau levels in the brain. Not applicable. A227A Frontotempora

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