ClinVar Miner

Submissions for variant NM_001282717.2(STAG3):c.2445T>A (p.Ile815=)

gnomAD frequency: 0.30556  dbSNP: rs1043915
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001616865 SCV001838196 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810139 SCV002057199 benign Premature ovarian failure 8 2021-07-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810140 SCV002057200 benign Spermatogenic failure 61 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001616865 SCV005267693 benign not provided criteria provided, single submitter not provided

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