RS63750579 APP

Health Risk Chr 21:25891856
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What This Variant Does
"APP gene mutations: either c.2077G&gt
Associated Conditions
ABeta amyloidosis
dutch type
Alzheimer disease
Cerebral amyloid angiopathy
APP-related
ABeta amyloidosis
Italian type
Alzheimer disease
ABeta amyloidosis
dutch type
Alzheimer disease
Cerebral amyloid angiopathy
APP-related
ABeta amyloidosis
Italian type
Other Variants in APP
rs63750264 rs63749964 rs63750671 rs281865161 rs63750066 rs63750399 rs63750734 rs63751039 rs63750973 rs63749810
Ask Dr. Hemsworth about this variant