ClinVar Miner

Submissions for variant NM_153252.5(BRWD3):c.5236C>T (p.Arg1746Ter) (rs868344048)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Hehr Laboratory,Center for Human Genetics - University of Regensburg RCV000681484 SCV000808934 uncertain significance Mental retardation, X-linked 93 2016-12-29 no assertion criteria provided clinical testing

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