RS778862698 PEX7

Health Risk Chr 6:136872196
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Rhizomelic chondrodysplasia punctata type 1
Peroxisome biogenesis disorder 9B
Nonpapillary renal cell carcinoma
Rhizomelic chondrodysplasia punctata type 1
Peroxisome biogenesis disorder 9B
Nonpapillary renal cell carcinoma
Other Variants in PEX7
rs1805137 rs121909151 rs121909152 rs121909153 rs63535662 rs148591292 rs121909154 rs267608255 rs61753238 rs61753233
Ask Dr. Hemsworth about this variant