RS747768373 FIG4
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4J
FIG4-related disorder
Inborn genetic diseases
Charcot-Marie-Tooth disease type 4
Charcot-Marie-Tooth disease type 4J
FIG4-related disorder
Other Variants in FIG4