ClinVar for Gene (Select 100132774) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3113783	NM_014663.3(KDM4A):c.2892A>T (p.Gln964His)	KDM4A, KDM4A-AS1 (Q964H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2672311	Single allele	A3GALT2, ACOT11 +1226 more	Inversion	Bilateral polymicrogyria	GLikely pathogenic
Select item 2622404	NM_014663.3(KDM4A):c.3100G>C (p.Glu1034Gln)	KDM4A, KDM4A-AS1 (E1034Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775543	NM_014663.3(KDM4A):c.2961+10G>A	KDM4A, KDM4A-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 741942	NM_014663.3(KDM4A):c.2922A>G (p.Gly974=)	KDM4A, KDM4A-AS1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 59966	GRCh38/hg38 1p34.2-34.1(chr1:40462415-44668040)x1	ARTN, ATP6V0B +279 more	Copy number loss	See cases	GPathogenic
Select item 57093	GRCh38/hg38 1p34.2-34.1(chr1:40693289-44514104)x1	ARTN, ATP6V0B +253 more	Copy number loss	See cases	GPathogenic

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