ClinVar Miner

Submissions for variant NM_007325.5(GRIA3):c.268+16762dup (rs11452643)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Mendelics	RCV000990936	SCV001142006	benign	Mental retardation, X-linked, syndromic, wu type	2019-05-28	criteria provided, single submitter	clinical testing

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