Related gene-specific medical variations for Gene (Select 79658) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1808370	GRCh37/hg19 4q31.23(chr4:148734569-148860556)x1	ARHGAP10	Copy number loss	not provided	GUncertain significance
Select item 562974	GRCh37/hg19 4q31.23(chr4:148765966-148840301)x1	ARHGAP10	Copy number loss	not provided	GUncertain significance
Select item 120315	NM_024605.4(ARHGAP10):c.2228A>G (p.His743Arg)	ARHGAP10 (H743R)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 120314	NM_024605.4(ARHGAP10):c.1468T>C (p.Ser490Pro)	ARHGAP10 (S490P)	Single nucleotide variant (missense variant)	not provided	Gnot provided
Select item 120313	NM_024605.4(ARHGAP10):c.1116+21A>G	ARHGAP10	Single nucleotide variant (intron variant)	not provided	Gnot provided
Select item 120312	NM_024605.4(ARHGAP10):c.822C>T (p.Val274=)	ARHGAP10	Single nucleotide variant (synonymous variant)	not provided	Gnot provided
Select item 120311	NM_024605.4(ARHGAP10):c.716T>A (p.Phe239Tyr)	ARHGAP10 (F239Y)	Single nucleotide variant (missense variant)	not provided	Gnot provided

ClinVar