List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000103.4(CYP19A1):c.1093C>T (p.Arg365Trp)	rs202076619	0.00001
NM_000103.4(CYP19A1):c.907A>G (p.Met303Val)	rs2031445857	0.00001
NM_000103.4(CYP19A1):c.1124G>T (p.Arg375Leu)	rs762631156
NM_000103.4(CYP19A1):c.1327G>A (p.Ala443Thr)
NM_000103.4(CYP19A1):c.230A>G (p.Tyr77Cys)	rs772620133

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