ClinVar Miner

Submissions for variant NM_001761.3(CCNF):c.1715G>T (p.Arg572Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004760285 SCV005374455 uncertain significance Frontotemporal dementia and/or amyotrophic lateral sclerosis 5 2024-09-22 criteria provided, single submitter clinical testing

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