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
rs1694068	ARL15			5	53987800	intron variant	T/A	snv	0.62	4
rs702634	ARL15	1.000	0.080	5	53975590	intron variant	G/A	snv	0.72	3
rs35951	ARL15	1.000	0.080	5	54296531	intron variant	G/T	snv	0.73	3
rs4865796	ARL15	1.000	0.080	5	53976834	intron variant	G/A	snv	0.72	3
rs6450176	ARL15			5	54002195	intron variant	G/A	snv	0.27	3
rs2441026	ARL15			5	54148668	intron variant	C/T	snv	0.44	2
rs111366116	ARL15			5	53999716	intron variant	C/T	snv	8.4E-02	2
rs7735249	ARL15			5	54014309	intron variant	C/G	snv	9.0E-02	2
rs11296991	ARL15			5	54012825	intron variant	TT/-;T;TTT	delins	0.29	2
rs114989019	ARL15			5	53898797	intron variant	C/T	snv	8.1E-03	2
rs16882447	ARL15			5	54207072	intron variant	C/A	snv	0.33	2
rs79760705	ARL15			5	54002886	intron variant	G/T	snv	8.5E-02	1
rs7719168	ARL15			5	53996560	intron variant	A/C	snv	8.7E-02	1
rs12186509	ARL15			5	54010860	intron variant	T/G	snv	0.28	1
rs3776712	ARL15			5	54008349	intron variant	T/C	snv	0.28	1
rs278064	ARL15			5	54163093	intron variant	T/C	snv	0.41	1
rs12654393	ARL15			5	54006790	intron variant	G/T	snv	0.27	1
rs16881971	ARL15			5	54005377	intron variant	T/C;G	snv		1
rs2448	ARL15			5	54006524	intron variant	T/C	snv	0.28	1
rs6874524	ARL15			5	54047699	intron variant	T/C	snv	0.31	1
rs28499105	ARL15			5	53978637	intron variant	G/A	snv	0.67	1
rs156380	ARL15			5	54082620	intron variant	T/A;C;G	snv		1
rs35006	ARL15	1.000	0.040	5	54146895	intron variant	C/G	snv	0.24	1
rs4311394	ARL15	1.000	0.080	5	54004832	intron variant	A/G	snv	0.27	1