"Ambry Genetics"[submitter] AND "LOC130008135"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2620687	NM_032496.4(ARHGAP9):c.764G>A (p.Gly255Asp)	ARHGAP9, LOC130008135 (G71D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312539	NM_032496.4(ARHGAP9):c.760C>A (p.Pro254Thr)	ARHGAP9, LOC130008135 (P70T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance