RS568067396 MAPT

Health Risk Chr 17:45991524
Upload your DNA to see your genotype for this variant.
Associated Conditions
MAPT-Related Spectrum Disorders
Inborn genetic diseases
MAPT-Related Spectrum Disorders
Inborn genetic diseases
Other Variants in MAPT
rs63751273 rs63750376 rs63750424 rs63750972 rs1568327531 rs63750570 rs63750756 rs63751165 rs63750512 rs63751438
Ask Dr. Hemsworth about this variant