List of variants in gene MAPT reported as pathogenic by Mendelics

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	gnomAD frequency
NM_001377265.1(MAPT):c.1972C>G (p.Leu658Val)	rs63750349
NM_001377265.1(MAPT):c.2064T>C (p.Asn688=)	rs63750912
NM_001377265.1(MAPT):c.2091T>C (p.Ser697=)	rs63750568

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