List of variants in gene MAPT reported as benign by Clinical Genetics, Academic 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: 17

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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.1941T>C (p.Asn647=)	rs17652121	0.14693
NM_001377265.1(MAPT):c.1091T>C (p.Val364Ala)	rs62063787	0.14671
NM_001377265.1(MAPT):c.220+2535A>G	rs1800547	0.14618
NM_001377265.1(MAPT):c.220+18C>T	rs75242405	0.14617
NM_001377265.1(MAPT):c.-13A>G	rs17650901	0.14470
NM_001377265.1(MAPT):c.1857A>G (p.Ala619=)	rs1052553	0.12790
NM_001377265.1(MAPT):c.1078G>A (p.Asp360Asn)	rs62063786	0.12772
NM_001377265.1(MAPT):c.830C>T (p.Pro277Leu)	rs63750417	0.12767
NM_001377265.1(MAPT):c.1564T>C (p.Ser522Pro)	rs10445337	0.12766
NM_001377265.1(MAPT):c.1732+2342T>C	rs62063845	0.12765
NM_001377265.1(MAPT):c.1704G>A (p.Pro568=)	rs1052551	0.12440
NM_001377265.1(MAPT):c.1333C>T (p.Arg445Trp)	rs17651549	0.12421
NM_001377265.1(MAPT):c.1080C>T (p.Asp360=)	rs63750222	0.11265
NM_001377265.1(MAPT):c.1178C>T (p.Ser393Leu)	rs73314997	0.05198
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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