ClinVar Miner

Submissions for variant NM_014629.4(ARHGEF10):c.141A>C (p.Pro47=) (rs4875950)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV000625165 SCV000743957 benign Slowed nerve conduction velocity, autosomal dominant 2017-07-28 criteria provided, single submitter clinical testing
Clinical Genetics,Academic Medical Center RCV001700416 SCV001925637 benign not specified no assertion criteria provided clinical testing

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