ClinVar Miner

List of variants reported as benign for Slowed nerve conduction velocity, autosomal dominant by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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Total variants: 5
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NM_014629.4(ARHGEF10):c.1075+13A>G rs4543586
NM_014629.4(ARHGEF10):c.2143+13T>G rs2294041
NM_014629.4(ARHGEF10):c.3398-16A>G rs7832438
NM_014629.4(ARHGEF10):c.387A>G (p.Val129=) rs749822
NM_014629.4(ARHGEF10):c.630G>A (p.Glu210=) rs7003969

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