"Genome-Nilou Lab"[submitter] AND "MIR4713HG"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 316469	NM_000103.4(CYP19A1):c.*19C>T	CYP19A1, MIR4713HG +1 more	Single nucleotide variant (3 prime UTR variant)	Aromatase excess syndrome +2 more	GBenign
Select item 316477	NM_000103.4(CYP19A1):c.240A>G (p.Val80=)	CYP19A1, MIR4713HG +1 more	Single nucleotide variant (synonymous variant)	Aromatase deficiency +2 more	GBenign