List of variants in gene MAPT reported as likely pathogenic for Frontotemporal dementia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP
NM_001377265.1(MAPT):c.2014AAG[1] (p.Lys673del)	rs63750688
NM_001377265.1(MAPT):c.2228A>G (p.Gln743Arg)	rs1568339821
NM_001377265.1(MAPT):c.2266C>A (p.Pro756Thr)	rs1598408336

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