RS202218688 APP

Health Risk Chr 21:26000131
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Associated Conditions
Alzheimer disease
Inborn genetic diseases
Alzheimer disease
Inborn genetic diseases
Other Variants in APP
rs63750579 rs63750264 rs63749964 rs63750671 rs281865161 rs63750066 rs63750399 rs63750734 rs63751039 rs63750973
Ask Dr. Hemsworth about this variant