Alzheimer Disease

Neurological 67 variants 7 genes

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Associated Genes (7)

TNF APP PSEN1 GRN MAPT CSF1R VCP

Associated Variants (67)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1800630	TNF	—	—	exploratory
RS202218688	APP	—	—	strong
RS1566657804	PSEN1	—	—	strong
RS1567885728	GRN	—	—	strong
RS1568339995	MAPT	—	—	strong
RS201269325	APP	—	—	strong
RS199890425	APP	—	—	strong
RS200088099	APP	—	—	strong
RS200103591	APP	—	—	strong
RS145371658	APP	—	—	strong
RS200978018	APP	—	—	strong
RS750279232	APP	—	—	strong
RS139819006	APP	—	—	strong
RS1566656702	PSEN1	—	—	strong
RS765657163	APP	—	—	strong
RS139885956	APP	—	—	strong
RS199723282	PSEN1	—	—	strong
RS201668897	APP	—	—	strong
RS768238394	APP	—	—	strong
RS201466202	APP	—	—	strong
RS752361848	APP	—	—	strong
RS2146237965	APP	—	—	strong
RS147485129	APP	—	—	strong
RS1305531440	APP	—	—	strong
RS372642708	APP	—	—	strong
RS761439332	APP	—	—	strong
RS193922916	APP	—	—	strong
RS63750579	APP	—	—	strong
RS63750264	APP	—	—	strong
RS63750671	APP	—	—	strong
RS281865161	APP	—	—	strong
RS63750066	APP	—	—	strong
RS63750399	APP	—	—	strong
RS63750734	APP	—	—	strong
RS63751039	APP	—	—	strong
RS63750973	APP	—	—	strong
RS63749810	APP	—	—	strong
RS63750643	APP	—	—	strong
RS63750009	PSEN1	—	—	strong
RS63750231	PSEN1	—	—	strong
RS63749891	PSEN1	—	—	strong
RS121917807	PSEN1	—	—	strong
RS63750886	PSEN1	—	—	strong
RS527890624	APP	—	—	strong
RS201290605	APP	—	—	strong
RS1561901881	CSF1R	—	—	strong
RS1561905293	CSF1R	—	—	strong
RS866101707	VCP	—	—	strong
RS1566630910	PSEN1	—	—	strong
RS1566638673	PSEN1	—	—	strong

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