RS184709736 INF2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Focal segmental glomerulosclerosis 5
Charcot-Marie-Tooth disease dominant intermediate E
Inborn genetic diseases
Kidney disorder
Focal segmental glomerulosclerosis 5
Charcot-Marie-Tooth disease dominant intermediate E
Inborn genetic diseases
Kidney disorder
Other Variants in INF2