ClinVar Miner

List of variants in gene PEX5 reported as likely benign for Zellweger syndrome

Included ClinVar conditions (32):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_001131025.1(PEX5):c.*20G>C rs145760932
NM_001131025.1(PEX5):c.*462G>C rs75145323
NM_001131025.1(PEX5):c.-210G>T rs117442311
NM_001131025.1(PEX5):c.-295T>C rs186539500
NM_001131025.1(PEX5):c.-332G>A rs146875386
NM_001131025.1(PEX5):c.1718+13A>G rs116873137
NM_001131026.2(PEX5):c.19+775_19+776dup rs112785895
NM_001351132.2(PEX5):c.*1097T>C
NM_001351132.2(PEX5):c.*114C>T
NM_001351132.2(PEX5):c.1053G>A (p.Leu351=) rs61740909

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