List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as benign for not specified

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000103.4(CYP19A1):c.*19C>T	rs10046	0.42803
NM_000103.4(CYP19A1):c.629-16T>G	rs4324076	0.42328
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.242A>G (p.Tyr81Cys)	rs199845027	0.00003

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