List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000103.4(CYP19A1):c.109T>C (p.Leu37=)	rs58282176	0.00583
NM_000103.4(CYP19A1):c.49G>A (p.Val17Met)	rs200111039	0.00031
NM_000103.4(CYP19A1):c.976C>T (p.Pro326Ser)	rs368902124	0.00011
NM_000103.4(CYP19A1):c.261C>T (p.Val87=)	rs1003379171

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