DisGeNET - a database of gene-disease associations

Results per page

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
rs398032702	C18orf25	18	46245574	intron variant	AA/-;A;AAA;AAAA;AAAAAAA;AAAAAAAAAAAAA	delins		4
rs3842397	C18orf25	18	46265918	3 prime UTR variant	TT/-	del	0.43	3
rs9944715	C18orf25	18	46251293	intron variant	A/G	snv	0.62	3
rs12963943	C18orf25	18	46225695	intron variant	C/T	snv	0.61	2
rs144667737	C18orf25	18	46189157	intron variant	G/A	snv	1.1E-02	2
rs3744858	C18orf25	18	46265306	3 prime UTR variant	C/T	snv	0.61	2
rs4890628	C18orf25	18	46208079	intron variant	T/C	snv	0.62	2
rs4890633	C18orf25	18	46253312	intron variant	G/A	snv	0.62	2
rs8095142	C18orf25	18	46213842	intron variant	G/A	snv	0.64	2
rs8095374	C18orf25	18	46213522	intron variant	T/C	snv	0.43	2
rs11082518	C18orf25	18	46262069	intron variant	G/A	snv	0.61	1
rs11356507	C18orf25	18	46236831	intron variant	TTTT/-;TT;TTT;TTTTT	delins		1
rs12605945	C18orf25	18	46254155	intron variant	A/G;T	snv		1
rs12607898	C18orf25	18	46222812	intron variant	A/G;T	snv		1
rs12962307	C18orf25	18	46235454	intron variant	A/G;T	snv		1
rs12969147	C18orf25	18	46226558	intron variant	G/A	snv	0.65	1
rs200351105	C18orf25	18	46262655	intron variant	-/AA	delins		1
rs4542747	C18orf25	18	46222203	intron variant	C/T	snv	0.66	1
rs4574015	C18orf25	18	46222160	intron variant	T/C	snv	0.73	1
rs4890317	C18orf25	18	46190544	intron variant	T/A;C	snv		1
rs4890319	C18orf25	18	46232678	3 prime UTR variant	T/A	snv	0.71	1
rs4890626	C18orf25	18	46204532	intron variant	G/C;T	snv		1
rs4890629	C18orf25	18	46217598	non coding transcript exon variant	A/G	snv	0.65	1
rs4890632	C18orf25	18	46246327	intron variant	G/A	snv	0.62	1
rs62098160	C18orf25	18	46252149	intron variant	T/A;C;G	snv		1