List of variants in gene MAPT reported as likely benign by CeGaT Praxis fuer Humangenetik Tuebingen

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
NM_001377265.1(MAPT):c.2091+29G>A	rs63751443
NM_001377265.1(MAPT):c.220+2477C>G
NM_001377265.1(MAPT):c.2349G>A (p.Glu783=)	rs142776675
NM_001377265.1(MAPT):c.963C>G (p.Pro321=)	rs550945297

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