ClinVar Miner

Submissions for variant NM_000044.6(AR):c.2633C>T (p.Thr878Ile)

dbSNP: rs137852580
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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 RCV000581272 SCV000692175 uncertain significance Androgen resistance syndrome 2009-05-11 no assertion criteria provided clinical testing

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