ClinVar Miner

List of variants in gene AKR1C3 reported as benign by Breakthrough Genomics, Breakthrough Genomics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_003739.6(AKR1C3):c.197G>A (p.Arg66Gln)	rs35961894	0.02492
NM_003739.6(AKR1C3):c.459G>A (p.Lys153=)	rs1937839	0.01694

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