"Revvity Omics, Revvity"[submitter] AND "LOC110011216"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 467745	NM_003924.4(PHOX2B):c.771GGC[3] (p.Ala260dup)	LOC110011216, PHOX2B	Microsatellite (inframe_insertion)	not provided +1 more	GUncertain significance
Select item 505021	NM_003924.4(PHOX2B):c.753_767dup (p.Ala256_Ala260dup)	LOC110011216, PHOX2B	Duplication (inframe_insertion)	not provided +3 more	GPathogenic
Select item 1323446	NM_003924.4(PHOX2B):c.726_743dup (p.Ala255_Ala260dup)	LOC110011216, PHOX2B	Duplication (inframe_insertion)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic

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