List of variants in gene MAPT reported as pathogenic by Invitae

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: 5

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HGVS	dbSNP
NM_001377265.1(MAPT):c.2013T>G (p.Asn671Lys)	rs63750756
NM_001377265.1(MAPT):c.2078C>T (p.Pro693Leu)	rs63751273
NM_001377265.1(MAPT):c.2091+16C>T	rs63751011
NM_001377265.1(MAPT):c.2185G>A (p.Val729Met)	rs63750570
NM_001377265.1(MAPT):c.2392C>T (p.Arg798Trp)	rs63750424

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