DisGeNET - a database of gene-disease associations

List of associated variants

Fibromyalgia, C0016053

Source: BEFREE ×

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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
rs35699176	ZNF77	1.000	0.080	19	2936537	stop gained	G/A	snv	3.1E-02	3.4E-02	1
rs3771863	TACR1 ; LOC105374811	0.925	0.240	2	75192588	intron variant	C/T	snv		0.30	2
rs25531	SLC6A4 ; LOC105371720	0.581	0.520	17	30237328	upstream gene variant	T/C	snv		0.18	72
rs1799971	OPRM1	0.559	0.600	6	154039662	missense variant	A/G	snv	0.19	0.12	95
rs5522	NR3C2	0.732	0.320	4	148436323	missense variant	C/T	snv	0.88	0.89	19
rs375382379	NR3C1	0.882	0.160	5	143399792	missense variant	T/C	snv	4.0E-06		5
rs550659379	NR3C1	0.882	0.160	5	143399780	missense variant	T/C	snv	4.0E-06	7.0E-06	5
rs752834812	NR3C1	0.882	0.160	5	143399885	missense variant	T/C	snv	8.0E-06		5
rs772651364	NR3C1	0.882	0.160	5	143400050	missense variant	C/T	snv	4.0E-06		5
rs1799983	NOS3	0.430	0.880	7	150999023	missense variant	T/A;G	snv	0.75		246
rs1314305899	NOS3	0.807	0.280	7	151003224	missense variant	C/T	snv	7.9E-06	2.1E-05	6
rs2297518	NOS2	0.658	0.480	17	27769571	missense variant	G/A	snv	0.18	0.17	29
rs11127292	MYT1L	0.925	0.160	2	2026171	intron variant	C/T	snv		0.11	2
rs1217691063	MTHFR	0.330	0.920	1	11796309	missense variant	A/G	snv	4.0E-06	7.0E-06	614
rs2097903	MGC4859 ; LOC107986766	1.000	0.080	7	10642782	intron variant	A/T	snv		0.51	1
rs224222	MEFV	0.724	0.440	16	3254463	missense variant	C/T	snv	0.24	0.21	15
rs1719152	LOC101927369 ; CCL4	1.000	0.080	17	36105271	missense variant	T/A	snv	0.21	0.18	1
rs562010289	LAMC2	0.925	0.120	1	183227583	missense variant	G/A;C	snv	1.7E-04		2
rs6313	HTR2A	0.562	0.640	13	46895805	synonymous variant	G/A	snv	0.41	0.40	82
rs6311	HTR2A	0.645	0.640	13	46897343	upstream gene variant	C/T	snv		0.40	41
rs75634836	HTR2A	0.807	0.160	13	46835532	missense variant	C/A;T	snv	4.0E-06		11
rs1043210477	GPX1	0.701	0.520	3	49358250	missense variant	G/A	snv			19
rs841	GCH1	0.827	0.200	14	54843774	splice region variant	G/A	snv	0.22	0.22	7
rs1800541	EDN1	0.851	0.120	6	12288986	upstream gene variant	T/G	snv		0.24	5
rs6280	DRD3	0.602	0.520	3	114171968	missense variant	C/T	snv	0.63	0.54	57