DisGeNET - a database of gene-disease associations

List of associated variants

Fatigue, C0015672

Source: ALL

Results per page

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
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	262
rs1800629	TNF	0.472	0.920	6	31575254	upstream gene variant	G/A	snv	0.12	0.14	169
rs1800795	IL6-AS1 ; IL6 ; STEAP1B	0.494	0.840	7	22727026	intron variant	C/G	snv		0.71	140
rs181109321	TTPA	0.776	0.320	8	63065904	splice region variant	C/A;T	snv	2.0E-05		17
rs1991517	LOC101928462 ; TSHR	0.752	0.240	14	81144239	missense variant	G/C	snv	0.90	0.91	13
rs199682734	OPRM1			6	154118718	synonymous variant	C/T	snv	8.1E-06	7.0E-06	1
rs2032582	ABCB1	0.538	0.800	7	87531302	missense variant	A/C;T	snv	0.54; 3.8E-02		97
rs2228145	IL6R	0.602	0.720	1	154454494	missense variant	A/C;T	snv	0.38; 1.2E-05		57
rs224222	MEFV	0.724	0.440	16	3254463	missense variant	C/T	snv	0.24	0.21	15
rs2287396	GSTZ1			14	77327849	non coding transcript exon variant	C/T	snv		0.15	1
rs2293052	NOS1	1.000	0.040	12	117277815	intron variant	G/A	snv		0.28	2
rs2295633	FAAH	0.827	0.120	1	46408711	intron variant	A/G;T	snv			7
rs25531	SLC6A4 ; LOC105371720	0.581	0.520	17	30237328	upstream gene variant	T/C	snv		0.18	72
rs267606640	AGL	0.882	0.120	1	99913557	stop gained	G/A	snv	5.6E-05	5.6E-05	5
rs2794521	CRP	0.742	0.480	1	159715306	upstream gene variant	C/T	snv		0.78	15
rs3087243	CTLA4	0.623	0.720	2	203874196	downstream gene variant	G/A	snv		0.37	44
rs3091244	CRP	0.724	0.280	1	159714875	upstream gene variant	G/A;T	snv			17
rs34778348	LRRK2 ; LOC105369736	0.742	0.120	12	40363526	missense variant	G/A	snv	1.7E-03	5.8E-04	15
rs36010656	SLCO1C1	0.925	0.080	12	20711408	missense variant	C/A;T	snv	3.4E-02		4
rs3740071	ABCC2			10	99830363	missense variant	G/A;C	snv	4.0E-06; 4.0E-06		1
rs3766246	FAAH			1	46399999	intron variant	A/C;G	snv			2
rs3783642	GCH1			14	54893485	intron variant	T/A;C	snv			2
rs387907170	ETFDH	0.925	0.080	4	158703436	missense variant	T/C	snv	4.0E-06		3
rs4129267	IL6R	0.807	0.200	1	154453788	intron variant	C/G;T	snv			13
rs4251961	IL1RN	0.763	0.200	2	113116890	intron variant	T/C	snv		0.29	10