ClinVar Miner

List of variants in gene PEX19 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: 10
Download table as spreadsheet
HGVS dbSNP
NM_002857.3(PEX19):c.*1084T>C rs77962224
NM_002857.3(PEX19):c.*2057T>G rs56089807
NM_002857.3(PEX19):c.*2353G>T rs9853
NM_002857.3(PEX19):c.*2637G>A rs41265787
NM_002857.3(PEX19):c.*328A>G rs115260345
NM_002857.3(PEX19):c.*487T>A rs16831724
NM_002857.3(PEX19):c.-14T>G rs2301297
NM_002857.3(PEX19):c.-41C>T rs113442137
NM_002857.3(PEX19):c.181-15A>G rs114403769
NM_002857.3(PEX19):c.879T>C (p.Gly293=) rs74125561

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.