DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Intelligence ×

Variants associated to the Gene: MAPT ×

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs8067056	MAPT	0.925	0.080	17	46006582	intron variant	T/C;G	snv		0.30	4
rs754593	MAPT	1.000	0.040	17	45977330	non coding transcript exon variant	G/A	snv		0.52	3
rs17563986	MAPT	1.000	0.040	17	45913906	intron variant	A/G	snv		0.14	1
rs242559	MAPT	1.000	0.080	17	45948522	intron variant	C/A	snv		0.71	1
rs28646281	MAPT			17	45900480	intron variant	T/C;G	snv			1
rs713522	MAPT			17	45987897	intron variant	T/C	snv		0.44	1
rs8065165	MAPT ; MAPT-AS1			17	45892951	intron variant	C/T	snv		0.12	1
rs2471738	STH ; MAPT	0.882	0.160	17	45998697	intron variant	C/T	snv		0.18	1