Variants in gene PEX10 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_002617.4(PEX10):c.291A>G (p.Thr97=)	rs2494598	0.74152
NM_002617.4(PEX10):c.279C>T (p.Gly93=)	rs1143016	0.05120
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.318G>A (p.Leu106=)	rs146452560	0.00649
NM_002617.4(PEX10):c.6C>G (p.Ala2=)	rs112471479	0.00523
NM_002617.4(PEX10):c.621C>G (p.Pro207=)	rs140107510	0.00350
NM_002617.4(PEX10):c.27G>A (p.Pro9=)	rs559431523	0.00018

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