ClinVar Miner

Submissions for variant NM_032656.4(DHX37):c.2177dup (p.Thr727fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laan Lab, Human Genetics Research Group, University of Tartu RCV003991646 SCV004239201 likely pathogenic Male infertility with azoospermia or oligozoospermia due to single gene mutation 2023-09-01 criteria provided, single submitter research

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