"GeneDx"[submitter] AND "KLHL9"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 152118	GRCh38/hg38 9p21.3(chr9:21150820-21517343)x3	IFNA1, IFNA10 +23 more	Copy number gain	See cases	GLikely benign
Select item 429781	NM_018847.4(KLHL9):c.560C>G (p.Thr187Ser)	KLHL9 (T187S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 426183	NM_018847.4(KLHL9):c.443G>A (p.Gly148Glu)	KLHL9 (G148E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 253667	GRCh37/hg19 9p24.3-13.1(chr9:213161-39092820)x3	ACER2, ACO1 +195 more	Copy number gain	See cases	GPathogenic
Select item 253633	GRCh37/hg19 9p24.3-13.1(chr9:163131-38763958)x3	ACER2, ACO1 +195 more	Copy number gain	See cases	GPathogenic
Select item 253592	GRCh37/hg19 9p24.3-11.2(chr9:213161-47212321)x4	ACER2, ACO1 +202 more	Copy number gain	See cases	GPathogenic
Select item 253402	GRCh37/hg19 9p24.3-q34.3(chr9:163131-141122114)x3	ABCA1, ABCA2 +771 more	Copy number gain	See cases	GPathogenic

ClinVar