DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Gene: NFKB1 ×

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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
rs28362491	LOC105377621 ; NFKB1	0.592	0.720	4	102500998	non coding transcript exon variant	ATTG/-	delins			56
rs3774937	NFKB1	0.776	0.280	4	102513096	intron variant	T/C	snv		0.26	9
rs4648068	NFKB1	0.790	0.240	4	102597148	intron variant	A/G	snv		0.31	9
rs113473633	NFKB1	1.000	0.040	4	102527974	intron variant	A/G	snv		1.6E-02	4
rs1598859	NFKB1	0.925	0.080	4	102585287	intron variant	T/C	snv		0.34	4
rs230521	NFKB1	0.851	0.160	4	102542171	intron variant	C/G	snv		0.59	4
rs230525	NFKB1	0.882	0.080	4	102537720	non coding transcript exon variant	G/A	snv		0.69	4
rs230530	NFKB1	0.882	0.080	4	102532823	intron variant	A/G	snv		0.37	4
rs3774934	NFKB1	0.851	0.080	4	102506319	intron variant	A/C;G;T	snv			4
rs147574894	NFKB1 ; LOC105377347	0.925	0.080	4	102600911	missense variant	A/G	snv	9.6E-05	3.9E-04	4
rs3774968	NFKB1 ; LOC105377347	0.882	0.120	4	102609955	intron variant	A/G	snv		0.64	4
rs4648127	LOC105377347 ; NFKB1	0.882	0.080	4	102614748	intron variant	C/T	snv		4.3E-02	3
rs774062108	LOC105377347 ; NFKB1	0.925	0.240	4	102607651	splice region variant	T/G	snv	4.0E-06		3
rs72696119	LOC105377621 ; NFKB1	0.925	0.120	4	102501347	5 prime UTR variant	C/G	snv		0.43	3
rs13117745	NFKB1	0.882	0.080	4	102557546	intron variant	C/T	snv		0.18	3
rs1801	NFKB1	0.882	0.080	4	102579897	intron variant	C/G;T	snv			3
rs230496	NFKB1	0.882	0.080	4	102567334	intron variant	G/A	snv		0.59	3
rs230534	NFKB1	0.882	0.120	4	102527884	intron variant	T/C	snv		0.73	3
rs230541	NFKB1	0.882	0.080	4	102576628	intron variant	G/A	snv		0.58	3
rs151134704	NFKB1 ; LOC105377347			4	102616435	splice region variant	C/T	snv	1.6E-04	9.1E-05	3
rs4648110	NFKB1 ; LOC105377347	0.925	0.080	4	102612664	intron variant	T/A	snv		0.22	3
rs4648143	LOC105377347 ; NFKB1	1.000	0.080	4	102616617	3 prime UTR variant	G/A;T	snv	5.0E-03; 4.0E-06		2
rs1020760	NFKB1	0.925	0.040	4	102593288	non coding transcript exon variant	C/G	snv		0.42	2
rs1241312324	NFKB1	0.925	0.200	4	102567083	missense variant	T/C	snv	4.0E-06		2
rs3774959	NFKB1	0.925	0.080	4	102589957	intron variant	G/A	snv		0.34	2