ClinVar Miner

Submissions for variant NM_000044.6(AR):c.2512G>A (p.Glu838Lys)

dbSNP: rs1555997775
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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 RCV000583039 SCV000692165 uncertain significance Androgen resistance syndrome 2016-06-29 no assertion criteria provided clinical testing

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