ClinVar Miner

Submissions for variant NM_001145073.3(USP27X):c.1141T>C (p.Tyr381His) (rs886038211)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000249317 SCV000301487 pathogenic Mental retardation, X-linked 105 2016-09-26 no assertion criteria provided literature only

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