DisGeNET - a database of gene-disease associations

List of shared variants

Alzheimer's Disease, C0002395

Disease: C-reactive protein measurement

Source: GWASCAT ×

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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
rs4420638	APOC1	0.708	0.520	19	44919689	downstream gene variant	A/G	snv		0.18	30
rs429358	APOE	0.590	0.600	19	44908684	missense variant	T/C	snv	0.14	0.16	26
rs2075650	TOMM40	0.662	0.360	19	44892362	intron variant	A/G	snv	0.13	0.13	12
rs6857	NECTIN2	0.790	0.240	19	44888997	3 prime UTR variant	C/T	snv		0.13	10
rs769449	APOE	0.882	0.120	19	44906745	non coding transcript exon variant	G/A	snv		8.4E-02	8
rs1160985	TOMM40	1.000	0.080	19	44900155	intron variant	C/T	snv		0.52	5
rs61812598	IL6R	1.000	0.080	1	154447611	intron variant	G/A	snv		0.31	4
rs157595		1.000	0.080	19	44922203	upstream gene variant	A/G;T	snv			3
rs1582763	MS4A4A	1.000	0.080	11	60254475	intron variant	G/A	snv		0.28	2