RS150420625 MAPT

Health Risk Chr 17:45991530
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Associated Conditions
Inborn genetic diseases
Frontotemporal dementia
Inborn genetic diseases
Frontotemporal dementia
Other Variants in MAPT
rs63751273 rs63750376 rs63750424 rs63750972 rs1568327531 rs63750570 rs63750756 rs63751165 rs63750512 rs63751438
Ask Dr. Hemsworth about this variant