ClinVar Miner

Submissions for variant NM_144605.5(SEPTIN12):c.266C>T (p.Thr89Met)

gnomAD frequency: 0.00004  dbSNP: rs199696526
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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
OMIM RCV000030756 SCV000053417 risk factor Spermatogenic failure 10 2012-04-01 no assertion criteria provided literature only
Reproductive Endocrinology and immunology College of Medicine, National Cheng Kung University RCV000030756 SCV000154686 not provided Spermatogenic failure 10 no assertion provided not provided

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