DisGeNET - a database of gene-disease associations

List of shared variants

Coronary Artery Disease, C1956346

Disease: Sepsis

Source: ALL

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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
rs11536889	TLR4	0.658	0.560	9	117715853	3 prime UTR variant	G/C	snv		0.11	27
rs1800777	CETP	0.724	0.280	16	56983407	missense variant	G/A	snv	3.7E-02	2.8E-02	17
rs3091244	CRP	0.724	0.280	1	159714875	upstream gene variant	G/A;T	snv			17
rs1129055	CD86	0.724	0.400	3	122119472	missense variant	G/A	snv	0.30	0.25	15
rs867186	PROCR ; MMP24-AS1-EDEM2	0.752	0.120	20	35176751	missense variant	A/G	snv	0.10	9.7E-02	15
rs10865710	PPARG	0.763	0.360	3	12311699	intron variant	C/G	snv		0.25	13
rs5743551	TLR1	0.742	0.240	4	38806033	intron variant	T/A;C	snv			12
rs2234237	TREM1	0.763	0.280	6	41282728	missense variant	T/A	snv	0.13	0.12	9
rs2234246	TREM1	0.827	0.240	6	41276002	3 prime UTR variant	C/T	snv		0.44	5
rs9770242	NAMPT	0.851	0.240	7	106285885	5 prime UTR variant	C/A	snv		0.79	5
rs2839693	CXCL12	0.882	0.120	10	44379119	intron variant	T/A;C	snv			3