List of variants in gene PEX10 reported as benign for not provided

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_002617.4(PEX10):c.601-235A>G	rs2494427	0.80929
NM_002617.4(PEX10):c.291A>G (p.Thr97=)	rs2494598	0.74152
NM_002617.4(PEX10):c.776+33G>T	rs3795269	0.38841
NM_002617.4(PEX10):c.*173G>A	rs1129171	0.27656
NM_002617.4(PEX10):c.913-4G>A	rs11586985	0.08566
NM_002617.4(PEX10):c.600+282T>C	rs76232811	0.05245
NM_002617.4(PEX10):c.279C>T (p.Gly93=)	rs1143016	0.05120
NM_002617.4(PEX10):c.601-324C>T	rs58827215	0.05049
NM_002617.4(PEX10):c.*11G>A	rs3795270	0.03427
NM_002617.4(PEX10):c.194-243del	rs142572177	0.02927
NM_002617.4(PEX10):c.820A>G (p.Thr274Ala)	rs34154371	0.01899
NM_001374426.1(PEX10):c.-321+994C>G	rs111413105	0.01014
NM_002617.4(PEX10):c.843G>A (p.Arg281=)	rs35082957	0.00846
NM_002617.4(PEX10):c.318G>A (p.Leu106=)	rs146452560	0.00649
NM_002617.4(PEX10):c.194-207G>A	rs12092052
NM_002617.4(PEX10):c.913-264G>C	rs2494426

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