Related gene-specific medical variations for Gene (Select 83592) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3065373	NM_001040177.3(AKR1E2):c.582+1G>A	AKR1E2	Single nucleotide variant (splice donor variant +1 more)	not provided	GUncertain significance
Select item 1316791	NM_001040177.3(AKR1E2):c.39+315T>C	AKR1E2, LOC130003192	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 815314	GRCh37/hg19 10p15.1(chr10:4652848-4893519)x3	AKR1E2	Copy number gain	not provided	GUncertain significance

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