List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as uncertain significance 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000103.4(CYP19A1):c.*125T>C	rs781742620	0.00024
NM_000103.4(CYP19A1):c.721T>A (p.Tyr241Asn)	rs143562020	0.00017
NM_000103.4(CYP19A1):c.*747G>A	rs866111735	0.00005

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