List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as pathogenic by GeneDx

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000103.4(CYP19A1):c.1051C>T (p.Gln351Ter)	rs781574524
NM_000103.4(CYP19A1):c.343C>T (p.Arg115Ter)	rs2141079375
NM_000103.4(CYP19A1):c.552T>G (p.Tyr184Ter)	rs2141062122

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