ClinVar Miner

Submissions for variant NM_001356.5(DDX3X):c.173C>G (p.Ser58Ter) (rs1602126980)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Mendelics	RCV000990794	SCV001141833	pathogenic	Mental retardation, X-linked 102	2019-05-28	criteria provided, single submitter	clinical testing

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