LOC130006761[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59772	GRCh38/hg38 11q22.1-25(chr11:100348599-135040246)x3	AASDHPPT, ABCG4 +1199 more	Copy number gain	See cases	GPathogenic
Select item 145533	GRCh38/hg38 11q23.1(chr11:111659380-112255732)x3	ALG9, BCO2 +45 more	Copy number gain	See cases	GUncertain significance
Select item 1210737	NM_001931.4(DLAT):c.-157G>A	DLAT, LOC130006761	Single nucleotide variant	not provided	GLikely benign
Select item 302447	NM_001931.4(DLAT):c.-156C>G	DLAT, LOC130006761	Single nucleotide variant	not provided	GLikely benign

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