List of variants in gene MAPT reported as pathogenic for Pick disease

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.2341G>A (p.Gly781Arg)	rs63750512	0.00001
NM_001377265.1(MAPT):c.1946A>C (p.Lys649Thr)	rs63750129
NM_001377265.1(MAPT):c.2135C>T (p.Ser712Phe)	rs63750635
NM_001377265.1(MAPT):c.2282A>T (p.Lys761Ile)	rs63751264

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