ClinVar Miner

Submissions for variant NM_000044.6(AR):c.2309T>G (p.Val770Gly)

dbSNP: rs1555996870
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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 RCV000581646 SCV000692161 uncertain significance Androgen resistance syndrome 2016-02-22 no assertion criteria provided clinical testing

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