C3808953[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 50501	NM_004309.6(ARHGDIA):c.547GAC[2] (p.Asp185del)	ARHGDIA (D185del +1 more)	Microsatellite (inframe_deletion +2 more)	Nephrotic syndrome, type 8	GPathogenic
Select item 140593	NM_004309.6(ARHGDIA):c.518G>T (p.Gly173Val)	ARHGDIA (G173V +1 more)	Single nucleotide variant (missense variant +2 more)	Nephrotic syndrome, type 8	GPathogenic
Select item 140594	NM_004309.6(ARHGDIA):c.358C>T (p.Arg120Ter)	ARHGDIA (R120* +1 more)	Single nucleotide variant (nonsense +1 more)	Nephrotic syndrome, type 8	GPathogenic

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