List of variants in gene AKR1C2 reported as uncertain significance for cardiomyopathy

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001393392.1(AKR1C2):c.158_159del (p.His53fs)	rs782217424	0.00031
NM_001393392.1(AKR1C2):c.487A>G (p.Ile163Val)
NM_001393392.1(AKR1C2):c.827_828del (p.Arg276fs)

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