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	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF GENOME	Num. diseases
rs1149833	DLEU1	0.925	0.160	13	50176740	intron variant	A/T	snv	0.47	2
rs117496431	DLEU1 ; DLEU7			13	50561606	intron variant	C/T	snv	8.5E-03	1
rs11842790	DLEU1			13	50350312	intron variant	C/T	snv	6.0E-02	1
rs123378	DLEU1	1.000	0.080	13	50514673	intron variant	G/A;C;T	snv		1
rs1239704	DLEU7 ; DLEU1			13	50578475	intron variant	G/A;T	snv		1
rs1239948	DLEU1 ; DLEU7			13	50532386	intron variant	A/T	snv	0.59	3
rs12429206	DLEU1			13	50871978	intron variant	A/G	snv	0.62	1
rs1262720	DLEU1 ; DLEU7			13	50610289	intron variant	G/A;T	snv		1
rs12853498	DLEU1			13	50339738	intron variant	T/A	snv	5.8E-02	1
rs12871645	DLEU1			13	50357429	intron variant	G/T	snv	3.8E-02	1
rs12874278	DLEU1			13	50361786	intron variant	C/T	snv	6.5E-02	1
rs12874827	DLEU1			13	50326600	intron variant	T/G	snv	5.5E-02	1
rs143794540	DLEU1			13	50277750	intron variant	A/G	snv	5.4E-03	1
rs1568672	DLEU1			13	50179268	intron variant	T/A	snv	0.13	1
rs157170	DLEU1			13	50508319	intron variant	A/G	snv	0.71	1
rs1638703	DLEU1	1.000	0.040	13	50514220	intron variant	G/C	snv	0.27	2
rs17074093	DLEU1			13	50314567	intron variant	A/G	snv	5.8E-02	1
rs17074143	DLEU1			13	50348637	intron variant	A/T	snv	5.8E-02	1
rs17074145	DLEU1			13	50355253	intron variant	G/C	snv	5.8E-02	1
rs17363566	DLEU1			13	50360756	intron variant	G/A	snv	6.5E-02	1
rs201798	DLEU1			13	50380585	intron variant	G/A	snv	0.52	1
rs202346	DLEU1			13	50513307	intron variant	C/A	snv	0.26	1
rs2066590	DLEU1 ; DLEU2			13	50127054	non coding transcript exon variant	G/A	snv	0.15	1
rs2066591	DLEU1			13	50134768	intron variant	T/C	snv	0.22	1
rs2687950	DLEU1			13	50144332	intron variant	C/T	snv	0.20	1