"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "ARHGEF15"[ - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 530551	NM_173728.4(ARHGEF15):c.54G>A (p.Arg18=)	ARHGEF15	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 242023	NM_173728.4(ARHGEF15):c.960G>A (p.Gln320=)	ARHGEF15	Single nucleotide variant (synonymous variant)	ARHGEF15-related condition +2 more	GBenign/Likely benign
Select item 412666	NM_173728.4(ARHGEF15):c.1250G>T (p.Arg417Leu)	ARHGEF15 (R417L)	Single nucleotide variant (missense variant)	See cases +2 more	GBenign/Likely benign

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ClinVar