RS63750399 APP

Health Risk Chr 21:25891787
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What This Variant Does
"rs63750399 represents two mutations in the APP gene. The c.2146A&gt
Associated Conditions
Alzheimer disease type 1
Alzheimer disease
Alzheimer disease type 1
Alzheimer disease
Other Variants in APP
rs63750579 rs63750264 rs63749964 rs63750671 rs281865161 rs63750066 rs63750734 rs63751039 rs63750973 rs63749810
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