RS63750869 MAPT

Health Risk Chr 17:46018707
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=4
Associated Conditions
Frontotemporal dementia
MAPT-related disorder
Frontotemporal dementia
MAPT-related disorder
Other Variants in MAPT
rs63751273 rs63750376 rs63750424 rs63750972 rs1568327531 rs63750570 rs63750756 rs63751165 rs63750512 rs63751438
Ask Dr. Hemsworth about this variant