ClinVar for Gene (Select 101928694) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1691082	NM_000236.3(LIPC):c.88+8149G>A	LIPC, LIPC-AS1	Single nucleotide variant (intron variant)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 1691081	NM_000236.3(LIPC):c.88+16269C>T	LIPC, LIPC-AS1	Single nucleotide variant (intron variant)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 57882	GRCh38/hg38 15q21.3-22.2(chr15:57567950-63019415)x1	ADAM10, ALDH1A2 +163 more	Copy number loss	See cases	GPathogenic
Select item 57881	GRCh38/hg38 15q21.2-22.2(chr15:50864913-59646577)x1	LOC130057143, LOC130057144 +287 more	Copy number loss	See cases	GPathogenic
Select item 57466	GRCh38/hg38 15q21.3(chr15:58227724-58464615)x1	LIPC, LIPC-AS1 +15 more	Copy number loss	See cases	GUncertain significance
Select item 57220	GRCh38/hg38 15q21.3-22.2(chr15:57456076-61907285)x1	ADAM10, ALDH1A2 +140 more	Copy number loss	See cases	GPathogenic
Select item 14455	NM_000236.3(LIPC):c.[88+16269C>T;88+8149G>A]	LIPC, LIPC-AS1	Single nucleotide variant (intron variant)	High density lipoprotein cholesterol level quantitative trait locus 12	Gassociation

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