ClinVar Miner

Submissions for variant NM_001377265.1(MAPT):c.2052C>T (p.Gly684=)

dbSNP: rs1598380419
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000920915 SCV001066303 likely benign not provided 2018-05-21 criteria provided, single submitter clinical testing

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