ClinVar Miner

Submissions for variant NM_153046.3(TDRD9):c.720_723del (p.Ser241fs)

dbSNP: rs765353898
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000678505 SCV000804572 pathogenic Spermatogenic failure 30 2025-05-23 no assertion criteria provided literature only
Genetics of Infertility and Preimplantation Genetic Diagnosis, Centre Hospitalier Universitaire Grenoble Alpes RCV001797124 SCV002039171 pathogenic Azoospermia 2021-12-20 no assertion criteria provided case-control

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