DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: DLEU1 ×

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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 GENOME	Num. diseases
rs9591325	DLEU1	0.851	0.080	13	50237084	intron variant	T/C	snv	6.0E-02	5
rs2812208	DLEU1			13	50132951	intron variant	G/A;C	snv		5
rs806321	DLEU1	0.851	0.160	13	50267187	intron variant	C/T	snv	0.47	4
rs1239948	DLEU1 ; DLEU7			13	50532386	intron variant	A/T	snv	0.59	3
rs1149833	DLEU1	0.925	0.160	13	50176740	intron variant	A/T	snv	0.47	2
rs806293	DLEU1			13	50238846	intron variant	T/A	snv	0.47	2
rs1638703	DLEU1	1.000	0.040	13	50514220	intron variant	G/C	snv	0.27	2
rs41284816	DLEU1 ; DLEU2			13	50081853	non coding transcript exon variant	G/C;T	snv		2
rs797487	DLEU1 ; DLEU7	0.925	0.040	13	50650173	intron variant	T/G	snv	0.56	2
rs6561599	DLEU1 ; RNASEH2B-AS1	1.000	0.040	13	50904782	non coding transcript exon variant	C/G	snv	0.61	2
rs797486	DLEU7 ; DLEU1			13	50647482	intron variant	C/A	snv	0.85	2
rs963740	DLEU7 ; DLEU1 ; DLEU1-AS1	1.000	0.080	13	50521959	intron variant	A/T	snv	0.28	2
rs1568672	DLEU1			13	50179268	intron variant	T/A	snv	0.13	1
rs806352	DLEU1			13	50289783	intron variant	T/G	snv	0.49	1
rs471315	DLEU1			13	50387357	intron variant	C/G;T	snv		1
rs157170	DLEU1			13	50508319	intron variant	A/G	snv	0.71	1
rs143794540	DLEU1			13	50277750	intron variant	A/G	snv	5.4E-03	1
rs41308558	DLEU1			13	50157231	non coding transcript exon variant	T/A;C;G	snv		1
rs2687950	DLEU1			13	50144332	intron variant	C/T	snv	0.20	1
rs74788384	DLEU1			13	50158288	intron variant	A/G	snv	7.5E-03	1
rs2762051	DLEU1	1.000	0.080	13	50261579	intron variant	C/T	snv	0.15	1
rs123378	DLEU1	1.000	0.080	13	50514673	intron variant	G/A;C;T	snv		1
rs3116590	DLEU1	1.000	0.040	13	50234741	intron variant	A/G	snv	0.21	1
rs9562955	DLEU1	1.000	0.040	13	50237019	intron variant	G/T	snv	6.4E-02	1
rs2066591	DLEU1			13	50134768	intron variant	T/C	snv	0.22	1