"Ambry Genetics"[submitter] AND "LINC01890"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2328079	NM_001007231.3(ARHGAP25):c.1834C>T (p.Arg612Cys)	ARHGAP25, LINC01890 (R611C +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594568	NM_001007231.3(ARHGAP25):c.1835G>A (p.Arg612His)	ARHGAP25, LINC01890 (R572H +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance