List of variants in gene PEX26 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001127649.3(PEX26):c.371+108C>T	rs464541	0.72214
NM_001127649.3(PEX26):c.*167G>A	rs464385	0.52045
NC_000022.11:g.18077804C>T	rs462055	0.28421
NM_001127649.3(PEX26):c.371+272G>A	rs17809735	0.07738
NC_000022.11:g.18077845T>G	rs12157958	0.05953
NM_001127649.3(PEX26):c.667+204C>T	rs75620601	0.02729
NM_001127649.3(PEX26):c.231-45T>G	rs114973307	0.01860
NM_001127649.3(PEX26):c.-363G>C	rs138787474	0.01598
NM_001127649.3(PEX26):c.*10C>T	rs117472525	0.01244
NM_001127649.3(PEX26):c.457C>G (p.Leu153Val)	rs12484657	0.01096
NM_001127649.3(PEX26):c.*2162G>A	rs45489191	0.00688

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