ClinVar Miner

Submissions for variant NM_153046.3(TDRD9):c.46A>C (p.Ile16Leu)

dbSNP: rs868220412
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001328691 SCV001519866 uncertain significance Spermatogenic failure 30 2020-02-14 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
Breakthrough Genomics, Breakthrough Genomics RCV004692519 SCV005193467 uncertain significance not provided criteria provided, single submitter not provided

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