List of variants in gene PEX6 reported as benign for Zellweger spectrum disorders

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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: 19

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HGVS	dbSNP	gnomAD frequency
NM_000287.4(PEX6):c.2814G>A (p.Glu938=)	rs1129186	0.56758
NM_000287.4(PEX6):c.399G>T (p.Val133=)	rs9462858	0.40130
NM_000287.4(PEX6):c.2816C>A (p.Pro939Gln)	rs1129187	0.40058
NM_000287.4(PEX6):c.883-3T>C	rs9986447	0.36088
NM_000287.4(PEX6):c.2426C>T (p.Ala809Val)	rs35830695	0.07211
NM_000287.4(PEX6):c.2364G>A (p.Val788=)	rs2274515	0.06152
NM_000287.4(PEX6):c.207C>T (p.Pro69=)	rs11539736	0.02141
NM_000287.4(PEX6):c.2644G>A (p.Val882Ile)	rs2274516	0.02095
NM_000287.4(PEX6):c.1028G>A (p.Arg343Gln)	rs111282915	0.01159
NM_000287.4(PEX6):c.1646C>T (p.Ala549Val)	rs115960224	0.00687
NM_000287.4(PEX6):c.2936C>T (p.Ala979Val)	rs115180949	0.00686
NM_000287.4(PEX6):c.210G>A (p.Gly70=)	rs398123304	0.00651
NM_000287.4(PEX6):c.2770G>T (p.Ala924Ser)	rs34551839	0.00619
NM_000287.4(PEX6):c.813G>T (p.Ala271=)	rs35503676	0.00544
NM_000287.4(PEX6):c.330C>G (p.Thr110=)	rs140486558	0.00513
NM_000287.4(PEX6):c.1480-5C>T	rs376473597	0.00157
NM_000287.4(PEX6):c.1677C>A (p.Asp559Glu)	rs61732159	0.00093
NM_000287.4(PEX6):c.853C>G (p.Pro285Ala)	rs61753220	0.00067
NM_000287.4(PEX6):c.1234-8_1234-7dup	rs200121485

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