ClinVar Miner

Submissions for variant NM_001761.3(CCNF):c.373G>A (p.Glu125Lys)

dbSNP: rs376056912
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Guerreiro-Bras Laboratory, Van Andel Institute RCV001848611 SCV002106325 likely pathogenic Frontotemporal dementia 2022-02-02 flagged submission research

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