List of variants in gene combination CYP19A1, MIR4713HG, PIRC66 reported as uncertain significance 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: 21

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HGVS	dbSNP	gnomAD frequency
NM_000103.4(CYP19A1):c.465C>T (p.Pro155=)	rs146495071	0.00012
NM_000103.4(CYP19A1):c.467G>A (p.Gly156Asp)	rs142652579	0.00009
NM_000103.4(CYP19A1):c.1221C>T (p.Phe407=)	rs764767709	0.00007
NM_000103.4(CYP19A1):c.1353C>T (p.Leu451=)	rs774940170	0.00006
NM_000103.4(CYP19A1):c.99C>A (p.Gly33=)	rs779177368	0.00004
NM_000103.4(CYP19A1):c.1263+8C>A	rs757404619	0.00003
NM_000103.4(CYP19A1):c.1387T>C (p.Leu463=)	rs377327265	0.00003
NM_000103.4(CYP19A1):c.237G>A (p.Arg79=)	rs749406233	0.00003
NM_000103.4(CYP19A1):c.1113C>T (p.Asp371=)	rs774007712	0.00002
NM_000103.4(CYP19A1):c.859-6G>T	rs756838912	0.00002
NM_000103.4(CYP19A1):c.1425C>T (p.His475=)	rs982752444	0.00001
NM_000103.4(CYP19A1):c.146-7G>T	rs1262602894	0.00001
NM_000103.4(CYP19A1):c.493G>A (p.Ala165Thr)	rs769769335	0.00001
NM_000103.4(CYP19A1):c.625G>A (p.Asp209Asn)	rs748459967	0.00001
NM_000103.4(CYP19A1):c.637A>G (p.Ile213Val)	rs1045354487	0.00001
NM_000103.4(CYP19A1):c.907A>G (p.Met303Val)	rs2031445857	0.00001
NM_000103.4(CYP19A1):c.1133T>C (p.Leu378Ser)	rs2031101006
NM_000103.4(CYP19A1):c.1212C>A (p.Leu404=)	rs772086882
NM_000103.4(CYP19A1):c.138A>C (p.Ser46=)	rs766042143
NM_000103.4(CYP19A1):c.196C>T (p.Leu66=)	rs2033435368
NM_000103.4(CYP19A1):c.228C>T (p.Tyr76=)	rs775978298

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