List of variants in gene PEX10 reported as likely 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_002617.4(PEX10):c.820A>G (p.Thr274Ala)	rs34154371	0.01899
NM_002617.4(PEX10):c.913-287C>T	rs55746053	0.01654
NM_001374426.1(PEX10):c.-321+994C>G	rs111413105	0.01014
NM_002617.4(PEX10):c.685G>C (p.Val229Leu)	rs139345520	0.00686
NM_002617.4(PEX10):c.318G>A (p.Leu106=)	rs146452560	0.00649
NM_002617.4(PEX10):c.113-26C>T	rs41315652	0.00590
NM_002617.4(PEX10):c.6C>G (p.Ala2=)	rs112471479	0.00523
NM_002617.4(PEX10):c.912+48G>A	rs139004865	0.00498
NM_002617.4(PEX10):c.112+89C>T	rs116441921	0.00406
NM_002617.4(PEX10):c.627G>A (p.Glu209=)	rs141430704	0.00043
NM_002617.4(PEX10):c.771C>T (p.His257=)	rs776503441	0.00006
NM_002617.4(PEX10):c.435G>A (p.Met145Ile)	rs368273118	0.00003
NM_002617.4(PEX10):c.897G>A (p.Ala299=)	rs372779905	0.00001
NM_001374426.1(PEX10):c.-321+950_-321+972dup	rs1405798424
NM_002617.4(PEX10):c.*102TC[1]	rs142006474
NM_002617.4(PEX10):c.113-62G>C
NM_002617.4(PEX10):c.601-19G>A	rs1570100790

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