ClinVar Miner

List of variants in gene MAPT reported as uncertain significance by GeneDx

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Total variants: 7
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HGVS dbSNP
NM_001377265.1(MAPT):c.1042T>C (p.Ser348Pro) rs753640366
NM_001377265.1(MAPT):c.110G>T (p.Gly37Val)
NM_001377265.1(MAPT):c.1115C>T (p.Ala372Val) rs377402921
NM_001377265.1(MAPT):c.1156G>A (p.Val386Met) rs747178896
NM_001377265.1(MAPT):c.1390G>A (p.Asp464Asn) rs768615863
NM_001377265.1(MAPT):c.1516G>A (p.Val506Met) rs375359117
NM_001377265.1(MAPT):c.898G>A (p.Asp300Asn)

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