List of variants in gene MAPT reported as likely benign by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.889C>A (p.Arg297Ser)	rs150983093	0.00038
NM_001377265.1(MAPT):c.220+2538C>G	rs368845248	0.00001
NM_001377265.1(MAPT):c.1326C>T (p.Pro442=)
NM_001377265.1(MAPT):c.220+2432G>A
NM_001377265.1(MAPT):c.220+2477C>G

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