List of variants in gene MAPT reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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.1546T>C (p.Tyr516His)	rs2258689	0.21570
NM_001377265.1(MAPT):c.1732+2342T>C	rs62063845	0.12765
NM_001377265.1(MAPT):c.914A>G (p.Gln305Arg)	rs63750072	0.03830
NM_001377265.1(MAPT):c.1986G>A (p.Pro662=)	rs11568305	0.03713

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