List of variants in gene MAPT reported as benign by PreventionGenetics,PreventionGenetics

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: 18

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HGVS	dbSNP
NM_001377265.1(MAPT):c.-13A>G	rs17650901
NM_001377265.1(MAPT):c.1078G>A (p.Asp360Asn)	rs62063786
NM_001377265.1(MAPT):c.1080C>T (p.Asp360=)	rs63750222
NM_001377265.1(MAPT):c.1091T>C (p.Val364Ala)	rs62063787
NM_001377265.1(MAPT):c.1178C>T (p.Ser393Leu)	rs73314997
NM_001377265.1(MAPT):c.1333C>T (p.Arg445Trp)	rs17651549
NM_001377265.1(MAPT):c.1546T>C (p.Tyr516His)	rs2258689
NM_001377265.1(MAPT):c.1564T>C (p.Ser522Pro)	rs10445337
NM_001377265.1(MAPT):c.1704G>A (p.Pro568=)	rs1052551
NM_001377265.1(MAPT):c.1708G>A (p.Ala570Thr)	rs63750612
NM_001377265.1(MAPT):c.1732+2342T>C	rs62063845
NM_001377265.1(MAPT):c.1857A>G (p.Ala619=)	rs1052553
NM_001377265.1(MAPT):c.1941T>C (p.Asn647=)	rs17652121
NM_001377265.1(MAPT):c.1986G>A (p.Pro662=)	rs11568305
NM_001377265.1(MAPT):c.220+18C>T	rs75242405
NM_001377265.1(MAPT):c.220+2535A>G	rs1800547
NM_001377265.1(MAPT):c.830C>T (p.Pro277Leu)	rs63750417
NM_001377265.1(MAPT):c.914A>G (p.Gln305Arg)	rs63750072

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