ClinVar for Gene (Select 100874200) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2253070	NM_001128615.2(ARHGEF3):c.70C>T (p.Arg24Trp)	ARHGEF3, ARHGEF3-AS1 (R24W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 60057	GRCh38/hg38 3p21.1-14.3(chr3:53287477-57025368)x1	ACTR8, ARHGEF3 +53 more	Copy number loss	See cases	GUncertain significance
Select item 57386	GRCh38/hg38 3p21.1-14.1(chr3:54045018-66060461)x1	ABHD6, ACOX2 +218 more	Copy number loss	See cases	GPathogenic

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