RS63751100 GRN

Health Risk Chr 17:44352088
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Associated Conditions
Neuronal ceroid lipofuscinosis 11
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
Inborn genetic diseases
Neuronal ceroid lipofuscinosis 11
GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
Inborn genetic diseases
Other Variants in GRN
rs63750077 rs63751006 rs63750331 rs606231220 rs63749801 rs606231221 rs63751243 rs63751294 rs63749877 rs2143337085
Ask Dr. Hemsworth about this variant