ClinVar Miner

Submissions for variant NM_004637.5(RAB7A):c.321C>T (p.Leu107=) (rs749227632)

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Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Invitae	RCV000639627	SCV000761206	likely benign	Charcot-Marie-Tooth disease, axonal, type 2b	2017-12-21	criteria provided, single submitter	clinical testing

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