ClinVar Miner

Submissions for variant NM_000044.6(AR):c.214C>T (p.Gln72Ter)

dbSNP: rs1555969512
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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 RCV000583962 SCV000692137 pathogenic Androgen resistance syndrome 2012-11-07 no assertion criteria provided clinical testing

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