"Ambry Genetics"[submitter] AND "RBP7"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2231330	NM_052960.3(RBP7):c.37A>G (p.Ser13Gly)	RBP7 (S13G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2389238	NM_052960.3(RBP7):c.169A>G (p.Ser57Gly)	RBP7 (S57G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3152602	NM_052960.3(RBP7):c.197A>C (p.Lys66Thr)	RBP7 (K66T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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