List of variants in gene MAPT reported as pathogenic for Progressive supranuclear ophthalmoplegia

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.2231C>T (p.Ser744Leu)	rs63750425	0.00001
NM_001377265.1(MAPT):c.14G>T (p.Arg5Leu)	rs63750959
NM_001377265.1(MAPT):c.2078C>T (p.Pro693Leu)	rs63751273
NM_001377265.1(MAPT):c.2084G>T (p.Gly695Val)	rs63751391

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