ClinVar Miner

List of variants in gene PEX26 reported as likely benign for Zellweger syndrome

Included ClinVar conditions (31):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_001199319.1(PEX26):c.-148C>T rs115617644
NM_017929.6(PEX26):c.*1003T>G rs79085553
NM_017929.6(PEX26):c.*10C>T rs117472525
NM_017929.6(PEX26):c.*1283C>T rs73876563
NM_017929.6(PEX26):c.*1590G>A rs5992169
NM_017929.6(PEX26):c.*1608G>A rs116824049
NM_017929.6(PEX26):c.*1623G>T rs114698763
NM_017929.6(PEX26):c.*1669C>G rs112015789
NM_017929.6(PEX26):c.*1778C>T rs79447039
NM_017929.6(PEX26):c.*1859A>C rs146739242
NM_017929.6(PEX26):c.*1957G>A rs11913772
NM_017929.6(PEX26):c.*2701G>C rs114075265
NM_017929.6(PEX26):c.*2878C>T rs116424707
NM_017929.6(PEX26):c.*400C>T rs74988725
NM_017929.6(PEX26):c.*464A>G rs141229564
NM_017929.6(PEX26):c.*692T>C rs79936154
NM_017929.6(PEX26):c.*754A>G rs114146293
NM_017929.6(PEX26):c.*917C>T rs9605518
NM_017929.6(PEX26):c.*943G>A rs79785382
NM_017929.6(PEX26):c.*944C>A rs78412274
NM_017929.6(PEX26):c.-115G>C rs138787474
NM_017929.6(PEX26):c.-82+12A>G rs62239019
NM_017929.6(PEX26):c.911G>A (p.Arg304His) rs17851387

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