Related gene-specific medical variations for Gene (Select 28232) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2685534	GRCh37/hg19 15q26.1(chr15:92679630-92773669)x1	SLCO3A1	Copy number loss	not provided	GUncertain significance
Select item 1691116	NM_013272.4(SLCO3A1):c.647-33581T>C	SLCO3A1	Single nucleotide variant (intron variant)	Vascular endothelial growth factor (VEGF) inhibitor response	Gassociation
Select item 503585	GRCh37/hg19 15q26.1(chr15:91935924-92575841)x3	SLCO3A1	Copy number gain	See cases	GUncertain significance

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