ClinVar Miner

Submissions for variant NM_201435.5(CCDC62):c.385G>C (p.Glu129Gln)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003120354 SCV003799424 uncertain significance Spermatogenic failure 67 2022-03-01 criteria provided, single submitter clinical testing

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