RS571301599 INF2

Health Risk Chr 14:104714836
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
Focal segmental glomerulosclerosis 5
Charcot-Marie-Tooth disease dominant intermediate E
Inborn genetic diseases
Other Variants in INF2
rs2140672369 rs267606877 rs267607183 rs267606878 rs267606879 rs267606880 rs387907034 rs387907035 rs387907036 rs387907037
Ask Dr. Hemsworth about this variant