List of variants in gene MAPT reported as uncertain significance by GeneDx

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: 8

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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.1042T>C (p.Ser348Pro)	rs753640366	0.00003
NM_001377265.1(MAPT):c.1390G>A (p.Asp464Asn)	rs768615863	0.00001
NM_001377265.1(MAPT):c.1516G>A (p.Val506Met)	rs375359117	0.00001
NM_001377265.1(MAPT):c.110G>T (p.Gly37Val)
NM_001377265.1(MAPT):c.1156G>A (p.Val386Met)	rs747178896
NM_001377265.1(MAPT):c.2495G>C (p.Gly832Ala)
NM_001377265.1(MAPT):c.898G>A (p.Asp300Asn)

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