RS61753238 PEX7
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What This Variant Does
"rs61753238, also known as Tyr40Ter or Y40X, is a mutation in the PEX7 gene on chromosome 6. The rare...
Associated Conditions
Peroxisome biogenesis disorder 9B
Rhizomelic chondrodysplasia punctata type 1
PEX7-related disorder
Phytanic acid storage disease
Rhizomelic chondrodysplasia punctata
Inborn genetic diseases
Peroxisome biogenesis disorder 9B
Rhizomelic chondrodysplasia punctata type 1
PEX7-related disorder
Phytanic acid storage disease
Rhizomelic chondrodysplasia punctata
Inborn genetic diseases
Other Variants in PEX7