ClinVar Miner

Submissions for variant NM_014629.4(ARHGEF10):c.630G>A (p.Glu210=) (rs7003969)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001613404 SCV001835817 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000608905 SCV000734598 benign Slowed nerve conduction velocity, autosomal dominant no assertion criteria provided clinical testing
Clinical Genetics,Academic Medical Center RCV001701118 SCV001923040 benign not specified no assertion criteria provided clinical testing

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