"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "RPS25"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 785892	NM_001028.3(RPS25):c.330C>T (p.Thr110=)	RPS25	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3244710	NC_000011.9:g.(?_118007742)_(119170491_?)del	ABCG4, ARCN1 +36 more	Deletion	not provided	GPathogenic
Select item 3244705	NC_000011.9:g.(?_118007742)_(119170491_?)dup	ABCG4, ARCN1 +36 more	Duplication	Atrial fibrillation, familial, 14	GUncertain significance
Select item 2422557	NC_000011.9:g.(?_117209303)_(120133495_?)dup	ABCG4, ARCN1 +54 more	Duplication	not provided	GUncertain significance
Select item 2422303	NC_000011.9:g.(?_116691583)_(121500272_?)dup	ABCG4, APOA1 +72 more	Duplication	RASopathy +5 more	GUncertain significance
Select item 1410294	NC_000011.9:g.(?_116660844)_(121500272_?)dup	RNF26, TAGLN +73 more	Duplication	not provided	GUncertain significance
Select item 1007237	NC_000011.9:g.(?_117856768)_(118972385_?)dup	CENATAC, CXCR5 +31 more	Duplication	Immunodeficiency 18 +4 more	GUncertain significance
Select item 831101	NC_000011.9:g.(?_117856768)_(118972385_?)del	PHLDB1, RPS25 +31 more	Deletion	Inflammatory bowel disease 28 +3 more	GPathogenic
Select item 659604	NC_000011.9:g.(?_118007722)_(119170511_?)del	DDX6, DPAGT1 +36 more	Deletion	Long QT syndrome 10	GUncertain significance

ClinVar