DisGeNET - a database of gene-disease associations

Source: GWASDB ×

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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
rs314268	LIN28B			6	104970103	intron variant	G/A	snv	0.64	2
rs167539	LIN28B			6	104962173	intron variant	C/A	snv	0.64	1
rs314262	LIN28B			6	104946746	intron variant	G/A	snv	0.46	1
rs314263	LIN28B			6	104944870	intron variant	C/T	snv	0.69	1
rs314273	LIN28B			6	105014007	intron variant	T/G	snv	0.64	1
rs314276	LIN28B	0.807	0.280	6	104960124	intron variant	A/C	snv	0.65	1
rs314280	LIN28B	0.925	0.040	6	104952962	intron variant	A/G	snv	0.46	1
rs364663	LIN28B			6	104995314	intron variant	T/A;G	snv		1
rs369065	LIN28B			6	104996183	intron variant	C/T	snv	0.63	1
rs395962	LIN28B			6	104949543	intron variant	T/G	snv	0.72	1
rs7759938	LIN28B-AS1	0.925	0.120	6	104931079	intron variant	C/T	snv	0.62	2
rs9391253	LIN28B-AS1			6	104919741	intron variant	A/T	snv	0.29	2
rs12200251	LIN28B-AS1			6	104934540	intron variant	G/A	snv	0.46	1
rs4946651	LIN28B-AS1			6	104921635	intron variant	A/G	snv	0.46	1
rs2095812	LIN28B ; LIN28B-AS1			6	104936103	non coding transcript exon variant	C/G	snv	0.31	1
rs7861820	LINC01505			9	106174393	intron variant	T/C	snv	0.62	2
rs10156597	LINC01505			9	106179228	intron variant	A/T	snv	0.36	1
rs10453225	LINC01505			9	106157939	intron variant	G/T	snv	0.36	1
rs10978430	LINC01505			9	106153728	intron variant	C/T	snv	0.33	1
rs12352703	LINC01505			9	106154985	intron variant	G/T	snv	0.32	1
rs12686569	LINC01505			9	106154430	intron variant	G/T	snv	0.30	1
rs1516881	LINC01505			9	106150773	intron variant	C/G;T	snv		1
rs1516882	LINC01505			9	106150630	intron variant	A/G	snv	0.32	1
rs1516883	LINC01505			9	106144986	intron variant	G/A	snv	0.32	1
rs1516890	LINC01505			9	106227118	intron variant	G/A	snv	0.56	1