List of variants in gene ATP7A 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_000052.7(ATP7A):c.2299G>C (p.Val767Leu)	rs2227291	0.24533
NM_000052.7(ATP7A):c.327G>A (p.Lys109=)	rs61747968	0.00978
NM_000052.7(ATP7A):c.1516A>G (p.Ile506Val)	rs143907597	0.00750
NM_000052.7(ATP7A):c.565A>G (p.Ile189Val)	rs2228447	0.00731
NM_000052.7(ATP7A):c.610+8G>A	rs144616937	0.00506
NM_000052.7(ATP7A):c.4201G>C (p.Val1401Leu)	rs5959130	0.00500
NM_000052.7(ATP7A):c.1823A>G (p.Tyr608Cys)	rs61742278	0.00380
NM_000052.7(ATP7A):c.3589A>G (p.Asn1197Asp)	rs148765730	0.00280
NM_000052.7(ATP7A):c.4390A>G (p.Ile1464Val)	rs2234938	0.00066
NM_000052.7(ATP7A):c.3210C>T (p.His1070=)	rs185917115	0.00012

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