List of variants in gene ARHGEF10 reported as benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_014629.4(ARHGEF10):c.3398-16A>G	rs7832438	0.93211
NM_014629.4(ARHGEF10):c.1075+13A>G	rs4543586	0.65298
NM_014629.4(ARHGEF10):c.2143+13T>G	rs2294041	0.28589
NM_014629.4(ARHGEF10):c.630G>A (p.Glu210=)	rs7003969	0.20504
NM_014629.4(ARHGEF10):c.387A>G (p.Val129=)	rs749822	0.05521

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