PEX2, peroxisomal biogenesis factor 2, 5828

N. diseases: 152; N. variants: 13
Disease: PEROXISOME BIOGENESIS DISORDER 5B ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267608188
rs267608188
Entrez Id: 5828
Gene Symbol: PEX2
PEX2
CUI: C3542026
Disease:
PEROXISOME BIOGENESIS DISORDER 5B 		C 0.700 GeneticVariation CLINVAR Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients. 17041890 2006