RS769120676 INF2

Health Risk Chr 14:104709654
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Associated Conditions
Inborn genetic diseases
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
Other Variants in INF2
rs2140672369 rs267606877 rs267607183 rs267606878 rs267606879 rs267606880 rs387907034 rs387907035 rs387907036 rs387907037
Ask Dr. Hemsworth about this variant