ClinVar Miner

List of variants in gene MAPT reported by Department of Pathology and Laboratory Medicine,Sinai Health System

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001377265.1(MAPT):c.896T>G (p.Val299Gly)	rs141120474	0.00235
NM_001377265.1(MAPT):c.1891G>A (p.Ala631Thr)	rs63750096	0.00067
NM_001377265.1(MAPT):c.889C>A (p.Arg297Ser)	rs150983093	0.00038

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