DisGeNET - a database of gene-disease associations

List of associated variants

Sepsis, C0243026

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
rs17446614	FOXO1	0.851	0.240	13	40565740	intron variant	G/A	snv		0.16	5
rs2069948	PROCR ; MMP24-AS1-EDEM2	0.851	0.160	20	35174686	non coding transcript exon variant	C/T	snv	0.55	0.62	5
rs2232618	LBP	0.851	0.160	20	38373117	missense variant	T/C	snv	9.2E-02	0.12	5
rs2857656	CCL2	0.851	0.120	17	34254988	upstream gene variant	G/A;C	snv			5
rs4957796	FER	0.851	0.120	5	109066439	intron variant	T/C	snv		0.16	5
rs9770242	NAMPT	0.851	0.240	7	106285885	5 prime UTR variant	C/A	snv		0.79	5
rs1524668	ADAM17	0.851	0.160	2	9557243	upstream gene variant	A/C	snv		0.64	4
rs2563298	TMCO6 ; CD14	0.851	0.200	5	140631730	3 prime UTR variant	C/A	snv		0.26	4
rs368287711	IL10RA	0.851	0.120	11	117989554	missense variant	C/A;T	snv	2.0E-05; 2.4E-05		4
rs11568821	LOC105373977 ; PDCD1	0.827	0.200	2	241851760	intron variant	C/G;T	snv			10
rs1126647	CXCL8	0.827	0.160	4	73743328	3 prime UTR variant	A/T	snv		0.31	8
rs121918094	TTR	0.827	0.280	18	31592921	missense variant	T/C	snv			8
rs212388	LOC112267968 ; LOC105378083	0.827	0.240	6	159069404	intron variant	C/G;T	snv			8
rs4358188	BPI	0.827	0.160	20	38318446	missense variant	G/A;C	snv	0.46		7
rs2297630	CXCL12	0.827	0.160	10	44376100	intron variant	G/A;T	snv		0.21	6
rs842647	REL	0.827	0.400	2	60892336	intron variant	G/A	snv		0.62	6
rs12692386	ADAM17	0.827	0.160	2	9555777	5 prime UTR variant	A/G	snv		0.72	5
rs13137	VMP1 ; MIR21	0.827	0.160	17	59841670	3 prime UTR variant	A/T	snv		0.18	5
rs2234246	TREM1	0.827	0.240	6	41276002	3 prime UTR variant	C/T	snv		0.44	5
rs1799768	SERPINE1	0.807	0.360	7	101126425	upstream gene variant	-/A;C	ins			6
rs353291	CARMN ; MIR145	0.807	0.200	5	149431183	non coding transcript exon variant	T/C	snv		0.35	6
rs1143643	IL1B	0.790	0.320	2	112830725	intron variant	C/T	snv		0.29	10
rs414171	MAPKAPK3 ; CISH	0.790	0.200	3	50612068	5 prime UTR variant	A/G;T	snv			9
rs4648068	NFKB1	0.790	0.240	4	102597148	intron variant	A/G	snv		0.31	9
rs11465996	LY96	0.790	0.240	8	73989727	upstream gene variant	C/G	snv		0.25	7