ClinVar Miner

Submissions for variant NM_015512.5(DNAH1):c.10765G>A (p.Asp3589Asn)

gnomAD frequency: 0.00006  dbSNP: rs200850423
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001502273 SCV001707101 likely benign Spermatogenic failure 18; Ciliary dyskinesia, primary, 37 2020-10-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001502273 SCV002804429 likely benign Spermatogenic failure 18; Ciliary dyskinesia, primary, 37 2022-01-05 criteria provided, single submitter clinical testing

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