DisGeNET - a database of gene-disease associations

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Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	Chr	Position	Consequence	Alleles	Class	AF GENOME	Num. diseases
rs2812208	DLEU1	13	50132951	intron variant	G/A;C	snv		5
rs1239948	DLEU1 ; DLEU7	13	50532386	intron variant	A/T	snv	0.59	3
rs41284816	DLEU1 ; DLEU2	13	50081853	non coding transcript exon variant	G/C;T	snv		2
rs806293	DLEU1	13	50238846	intron variant	T/A	snv	0.47	2
rs797486	DLEU7 ; DLEU1	13	50647482	intron variant	C/A	snv	0.85	2
rs1239704	DLEU7 ; DLEU1	13	50578475	intron variant	G/A;T	snv		1
rs1568672	DLEU1	13	50179268	intron variant	T/A	snv	0.13	1
rs3116602	DLEU1 ; DLEU7	13	50537219	intron variant	T/G	snv	0.15	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
rs3118917	DLEU7 ; DLEU1	13	50571933	intron variant	C/A;T	snv	3.9E-02	1
rs3118905	DLEU1 ; DLEU7	13	50531198	intron variant	G/A	snv	0.21	1
rs143794540	DLEU1	13	50277750	intron variant	A/G	snv	5.4E-03	1
rs3118906	DLEU1 ; DLEU7	13	50532652	intron variant	G/A	snv	0.21	1
rs3118077	LOC107984567 ; DLEU7 ; DLEU1	13	50728174	intron variant	G/A	snv	0.74	1
rs3116614	DLEU7 ; DLEU1	13	50576594	intron variant	A/C	snv	0.24	1
rs41308558	DLEU1	13	50157231	non coding transcript exon variant	T/A;C;G	snv		1
rs386363597	DLEU1 ; DLEU7	13	50657252	intron variant	-/C	delins	1.4E-05	1
rs3118914	DLEU7 ; DLEU1	13	50542765	intron variant	G/T	snv	0.15	1
rs475883	DLEU1 ; DLEU7	13	50599596	intron variant	G/C	snv	0.13	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
rs978332	DLEU7 ; DLEU1	13	50562603	intron variant	C/T	snv	0.69	1
rs2066591	DLEU1	13	50134768	intron variant	T/C	snv	0.22	1