"GeneDx"[submitter] AND "LOC130061159"[gene] - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59589	GRCh38/hg38 17q21.32-22(chr17:49137864-52147810)x1	ABCC3, ABI3 +203 more	Copy number loss	See cases	GPathogenic
Select item 1227828	NC_000017.11:g.50345953G>A	LOC130061159, XYLT2	Single nucleotide variant	not provided	GBenign
Select item 1294957	NC_000017.11:g.50346057G>C	LOC130061159, XYLT2	Single nucleotide variant	not provided	GBenign
Select item 1179491	NC_000017.11:g.50346057G>A	LOC130061159, XYLT2	Single nucleotide variant	not provided	GBenign
Select item 1264676	NC_000017.11:g.50346069G>C	LOC130061159, XYLT2	Single nucleotide variant	not provided	GBenign

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