DisGeNET - a database of gene-disease associations

List of associated variants

Septicemia, C0036690

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
rs747126003	IL6-AS1 ; IL6	0.689	0.400	7	22728790	missense variant	A/G;T	snv	4.0E-06		18
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
rs7096206	MBL2	0.708	0.480	10	52771925	upstream gene variant	G/A;C;T	snv			17
rs1360485	HMGB1	0.742	0.320	13	30457747	3 prime UTR variant	C/T	snv		0.58	16
rs885479	MC1R	0.732	0.280	16	89919746	missense variant	G/A	snv	0.15	8.3E-02	16
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
rs34557412	TNFRSF13B	0.763	0.240	17	16948873	missense variant	A/G	snv	3.5E-03	3.9E-03	15
rs2808630		0.742	0.240	1	159711078	downstream gene variant	C/T	snv		0.77	13
rs1799946	DEFB1	0.732	0.360	8	6877909	5 prime UTR variant	C/T	snv	0.36	0.41	13
rs61330082	NAMPT	0.732	0.320	7	106286419	upstream gene variant	G/A	snv		0.22	13
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
rs510432	ATG5	0.752	0.280	6	106326155	upstream gene variant	T/C	snv		0.57	11
rs17281995	CD86	0.763	0.360	3	122120794	3 prime UTR variant	G/A;C	snv			11
rs12508721	IL21-AS1	0.742	0.360	4	122623509	intron variant	C/T	snv		0.24	11
rs653765	ADAM10	0.763	0.240	15	58749813	upstream gene variant	T/C;G	snv		0.45	10
rs1143643	IL1B	0.790	0.320	2	112830725	intron variant	C/T	snv		0.29	10
rs11568821	LOC105373977 ; PDCD1	0.827	0.200	2	241851760	intron variant	C/G;T	snv			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
rs2234237	TREM1	0.763	0.280	6	41282728	missense variant	T/A	snv	0.13	0.12	9
rs1126647	CXCL8	0.827	0.160	4	73743328	3 prime UTR variant	A/T	snv		0.31	8
rs212388	LOC112267968 ; LOC105378083	0.827	0.240	6	159069404	intron variant	C/G;T	snv			8