ClinVar Miner

Submissions for variant NM_000044.6(AR):c.1768+2T>C (rs1555982894)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GenePathDx,Causeway Health Care Private Ltd RCV000517655 SCV000616339 likely pathogenic Partial androgen insensitivity syndrome 2017-08-02 criteria provided, single submitter clinical testing
Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospital RCV000583701 SCV000692148 pathogenic Androgen resistance syndrome 2013-04-09 no assertion criteria provided clinical testing

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