ClinVar Miner

Submissions for variant NM_014629.4(ARHGEF10):c.474C>T (p.Asp158=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000900507 SCV001044827 benign not provided 2018-04-30 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001862 SCV001159579 benign Slowed nerve conduction velocity, autosomal dominant 2018-08-09 criteria provided, single submitter clinical testing

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