RS267608255 PEX7
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What This Variant Does
"PEX7 IVS3, A-G, -10 Rhizomelic chondrodysplasia punctata type 1 This SNP is called i5006215 by 23and...
Associated Conditions
Peroxisome biogenesis disorder 9B
Phytanic acid storage disease
Rhizomelic chondrodysplasia punctata type 1
Retinal dystrophy
Inborn genetic diseases
Peroxisome biogenesis disorder
Peroxisome biogenesis disorder 9B
Phytanic acid storage disease
Rhizomelic chondrodysplasia punctata type 1
Retinal dystrophy
Inborn genetic diseases
Peroxisome biogenesis disorder
Other Variants in PEX7