List of variants in gene MAPT reported as benign by Athena Diagnostics Inc

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.1857A>G (p.Ala619=)	rs1052553	0.14782
NM_001377265.1(MAPT):c.1941T>C (p.Asn647=)	rs17652121	0.14693
NM_001377265.1(MAPT):c.220+2535A>G	rs1800547	0.14618
NM_001377265.1(MAPT):c.1704G>A (p.Pro568=)	rs1052551	0.12440
NM_001377265.1(MAPT):c.1986G>A (p.Pro662=)	rs11568305	0.03866
NM_001377265.1(MAPT):c.1708G>A (p.Ala570Thr)	rs63750612	0.01528
NM_001377265.1(MAPT):c.2091+29G>A	rs63751443	0.00213
NM_001377265.1(MAPT):c.1938G>A (p.Lys646=)	rs141636979	0.00009
NM_001377265.1(MAPT):c.2091+25C>T	rs63750117	0.00003

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