"Ambry Genetics"[submitter] AND "LOC129932089"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2544524	NM_005717.4(ARPC5):c.96C>A (p.Asp32Glu)	ARPC5, LOC129932089 (D32E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3129805	NM_005717.4(ARPC5):c.5C>G (p.Ser2Trp)	ARPC5, LOC129932089 (S2W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance