List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as benign by Natera, Inc.

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000103.4(CYP19A1):c.*161T>G	rs4646	0.70442
NM_000103.4(CYP19A1):c.240A>G (p.Val80=)	rs700518	0.39685
NM_000103.4(CYP19A1):c.790C>T (p.Arg264Cys)	rs700519	0.08141
NM_000103.4(CYP19A1):c.602C>T (p.Thr201Met)	rs28757184	0.03608
NM_000103.4(CYP19A1):c.186C>T (p.His62=)	rs60308277	0.02885
NM_000103.4(CYP19A1):c.451+8G>A	rs28892004	0.00118
NM_000103.4(CYP19A1):c.475C>T (p.Arg159Cys)	rs201842322	0.00047
NM_000103.4(CYP19A1):c.75C>T (p.Thr25=)	rs745979108	0.00010
NM_000103.4(CYP19A1):c.1224C>T (p.Pro408=)	rs2304461	0.00009
NM_000103.4(CYP19A1):c.1370G>A (p.Arg457Gln)	rs770120065

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