ClinVar Miner

Submissions for variant NM_001282717.2(STAG3):c.1293A>C (p.Pro431=)

dbSNP: rs3735241
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001648252 SCV001856151 benign not provided 2021-05-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810181 SCV002057195 benign Premature ovarian failure 8 2021-07-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001810182 SCV002057196 benign Spermatogenic failure 61 2021-07-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001648252 SCV005267690 benign not provided criteria provided, single submitter not provided

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