ClinVar Miner

Submissions for variant NM_003140.3(SRY):c.266A>C (p.Glu89Ala)

dbSNP: rs1556370554
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital RCV000583608 SCV000692403 uncertain significance 46,XY sex reversal 1 2009-04-30 no assertion criteria provided clinical testing

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