ClinVar Miner

List of variants in gene MAPT studied for Frontotemporal dementia; Parkinson disease, late-onset; Progressive supranuclear palsy-parkinsonism syndrome; Pick disease; 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
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.1115C>T (p.Ala372Val)	rs377402921	0.00010
NM_001377265.1(MAPT):c.2013T>G (p.Asn671Lys)	rs63750756
NM_001377265.1(MAPT):c.2078C>T (p.Pro693Leu)	rs63751273

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