ClinVar Miner

List of variants in gene MAPT reported as likely pathogenic for Grn-related frontotemporal lobar degeneration with Tdp43 inclusions

Included ClinVar conditions (12):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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NM_016835.4(MAPT):c.1789_1791AAG[1] (p.Lys598del) rs63750688
NM_016835.4(MAPT):c.2003A>G (p.Gln668Arg) rs1568339821
NM_016835.4(MAPT):c.2041C>A (p.Pro681Thr) rs1598408336

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