ClinVar Miner

Submissions for variant NM_014629.4(ARHGEF10):c.1260+4C>T (rs79548709)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000975173 SCV001123052 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001001937 SCV001159708 benign Slowed nerve conduction velocity, autosomal dominant 2018-11-15 criteria provided, single submitter clinical testing

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