List of variants in gene ATP7B reported as benign by Eurofins NTD LLC (GA)

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_000053.4(ATP7B):c.3419T>C (p.Val1140Ala)	rs1801249	0.57256
NM_000053.4(ATP7B):c.2855G>A (p.Arg952Lys)	rs732774	0.56484
NM_000053.4(ATP7B):c.2495A>G (p.Lys832Arg)	rs1061472	0.54674
NM_000053.4(ATP7B):c.3903+6C>T	rs2282057	0.53754
NM_000053.4(ATP7B):c.1366G>C (p.Val456Leu)	rs1801244	0.41941
NM_000053.4(ATP7B):c.1216T>G (p.Ser406Ala)	rs1801243	0.41549
NM_000053.4(ATP7B):c.2866-13G>C	rs7325983	0.10642
NM_000053.4(ATP7B):c.2973G>A (p.Thr991=)	rs1801246	0.04852
NM_000053.4(ATP7B):c.3009G>A (p.Ala1003=)	rs1801247	0.04023
NM_000053.4(ATP7B):c.3620A>G (p.His1207Arg)	rs7334118	0.02828
NM_000053.4(ATP7B):c.4311G>A (p.Lys1437=)	rs73202048	0.00732
NM_000053.4(ATP7B):c.3369G>A (p.Pro1123=)	rs61733679	0.00362
NM_000053.4(ATP7B):c.1607T>C (p.Val536Ala)	rs138427376	0.00342
NM_000053.4(ATP7B):c.3060+16G>T	rs76163470	0.00196
NM_000053.4(ATP7B):c.3889G>A (p.Val1297Ile)	rs148399850	0.00192
NM_000053.4(ATP7B):c.2785A>G (p.Ile929Val)	rs534960245	0.00038
NM_000053.4(ATP7B):c.2310C>G (p.Leu770=)	rs398123136	0.00005

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