List of variants in gene ARHGEF10 reported as benign for Charcot-Marie-Tooth disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP
NM_014629.4(ARHGEF10):c.1075+13A>G	rs4543586
NM_014629.4(ARHGEF10):c.1110G>C (p.Leu370Phe)	rs9657362
NM_014629.4(ARHGEF10):c.1113C>T (p.Phe371=)	rs34655804
NM_014629.4(ARHGEF10):c.1260+4C>T	rs79548709
NM_014629.4(ARHGEF10):c.141A>C (p.Pro47=)	rs4875950
NM_014629.4(ARHGEF10):c.1991T>C (p.Met664Thr)	rs34319003
NM_014629.4(ARHGEF10):c.2098G>A (p.Val700Ile)	rs2294039
NM_014629.4(ARHGEF10):c.2143+13T>G	rs2294041
NM_014629.4(ARHGEF10):c.3398-16A>G	rs7832438
NM_014629.4(ARHGEF10):c.38-10T>C	rs138713415
NM_014629.4(ARHGEF10):c.387A>G (p.Val129=)	rs749822
NM_014629.4(ARHGEF10):c.474C>T (p.Asp158=)	rs147914724
NM_014629.4(ARHGEF10):c.630G>A (p.Glu210=)	rs7003969

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