RS63750004 PSEN1

Health Risk Chr 14:73173655
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs63750004, also known as c.428T&gt
Associated Conditions
Pick disease
Frontotemporal dementia
Alzheimer disease 3
Acne inversa
familial
3
Pick disease
Frontotemporal dementia
Alzheimer disease 3
Acne inversa
familial
3
Other Variants in PSEN1
rs63750306 rs63750590 rs63750526 rs63751235 rs661 rs63751037 rs63749885 rs63750231 rs63751229 rs63751272
Ask Dr. Hemsworth about this variant