List of variants in gene MAPT reported as likely pathogenic

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.2263G>A (p.Val755Ile)	rs63750869	0.00006
NM_001377265.1(MAPT):c.2091+19C>G	rs63750162	0.00001
NM_001377265.1(MAPT):c.2341G>A (p.Gly781Arg)	rs63750512	0.00001
NM_001377265.1(MAPT):c.2014AAG[1] (p.Lys673del)	rs63750688
NM_001377265.1(MAPT):c.2064T>C (p.Asn688=)	rs63750912
NM_001377265.1(MAPT):c.2091T>C (p.Ser697=)	rs63750568
NM_001377265.1(MAPT):c.2228A>G (p.Gln743Arg)	rs1568339821
NM_001377265.1(MAPT):c.2242T>A (p.Ser748Thr)	rs2076339915
NM_001377265.1(MAPT):c.2260C>T (p.His754Tyr)	rs1568339995
NM_001377265.1(MAPT):c.2266C>A (p.Pro756Thr)	rs1598408336

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