"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ARHGAP45"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2648899	NM_012292.5(ARHGAP45):c.2292C>T (p.Ser764=)	ARHGAP45	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2648900	NM_012292.5(ARHGAP45):c.2667T>G (p.Gly889=)	ARHGAP45	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 444854	GRCh37/hg19 19p13.3(chr19:266117-1094614)x3	ABCA7, ARHGAP45 +34 more	Copy number gain	not provided	GLikely pathogenic

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