Related gene-specific medical variations for Gene (Select 133482) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 814719	GRCh37/hg19 5q21.1(chr5:101766705-101865789)x1	SLCO6A1	Copy number loss	not provided	GLikely benign
Select item 563096	GRCh37/hg19 5q21.1(chr5:101821498-101961032)x1	SLCO6A1	Copy number loss	not provided	GUncertain significance
Select item 151629	GRCh38/hg38 5q21.1(chr5:102304556-102388761)x3	SLCO6A1	Copy number gain	See cases	GLikely benign
Select item 147612	GRCh38/hg38 5q21.1(chr5:102458385-102498538)x1	SLCO6A1	Copy number loss	See cases	GBenign

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