List of variants in gene MAPT reported as pathogenic for not provided

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: 6

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HGVS	dbSNP
NM_001377265.1(MAPT):c.2060ATA[1] (p.Asn688del)	rs63751392
NM_001377265.1(MAPT):c.2078C>T (p.Pro693Leu)	rs63751273
NM_001377265.1(MAPT):c.2091+16C>T	rs63751011
NM_001377265.1(MAPT):c.2091+3G>A	rs63750013
NM_001377265.1(MAPT):c.2120T>G (p.Leu707Arg)	rs63749855
NM_001377265.1(MAPT):c.2392C>T (p.Arg798Trp)	rs63750424

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