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
rs514716	GLIS3	1.000	0.080	9	3929424	intron variant	C/A;T	snv		1
rs1983753	GLIS3			9	4160364	intron variant	G/A;C	snv		1
rs7020673	GLIS3	0.882	0.200	9	4291747	intron variant	C/A;G	snv		1
rs6476839	GLIS3	0.925	0.120	9	4290823	intron variant	A/C;T	snv		1
rs10758593	GLIS3	0.827	0.240	9	4292083	intron variant	G/A	snv	0.45	1
rs1017568	GLIS3	1.000	0.080	9	3948365	intron variant	T/C;G	snv		1
rs7041847	GLIS3	1.000	0.080	9	4287466	intron variant	A/G	snv	0.37	1
rs7872188	GLIS3			9	4124377	intron variant	C/T	snv	0.36	1
rs736893	GLIS3	0.925	0.040	9	4217028	intron variant	G/A;C	snv		1
rs501461	GLIS3			9	4039727	intron variant	G/A;T	snv		1
rs10114763	GLIS3	1.000	0.040	9	4143749	intron variant	A/T	snv	0.39	1
rs13301469	GLIS3	1.000	0.040	9	3911353	intron variant	C/G	snv	0.17	1
rs12348139	GLIS3			9	4232743	intron variant	T/C	snv	7.9E-02	1
rs1570204	GLIS3			9	4216751	intron variant	T/C	snv	0.25	1
rs2224492	GLIS3			9	4237546	intron variant	A/G	snv	0.25	1
rs7047871	GLIS3			9	4050113	intron variant	T/A	snv	0.30	1
rs6476827	GLIS3			9	4220832	intron variant	C/G	snv	0.24	1
rs4741893	GLIS3			9	4123284	intron variant	G/A;C	snv		1
rs10119187	GLIS3			9	4223660	intron variant	T/C;G	snv	0.22	1
rs12336359	GLIS3			9	4129657	intron variant	G/C	snv	0.37	1
rs4237150	GLIS3			9	4290085	intron variant	G/A;C;T	snv		1
rs10974256	GLIS3			9	3952892	intron variant	G/A;C	snv		1
rs10974406	GLIS3			9	4237041	intron variant	T/C	snv	0.29	1
rs10974399	GLIS3			9	4232588	intron variant	G/T	snv	0.40	1
rs28558845	GLIS3			9	4334791	intron variant	G/A;C;T	snv		1