DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: HNF1B ×

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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 EXOME	AF GENOME	Num. diseases
rs12601991	HNF1B	0.708	0.280	17	37741642	intron variant	T/A;G	snv			17
rs11651052	HNF1B	0.851	0.200	17	37742390	intron variant	G/A	snv		0.50	7
rs4430796	HNF1B	0.790	0.280	17	37738049	intron variant	A/G	snv		0.52	4
rs11651755	HNF1B	0.763	0.160	17	37739849	intron variant	T/C	snv		0.52	4
rs7501939	HNF1B	0.776	0.280	17	37741165	intron variant	C/T	snv		0.41	3
rs7405776	HNF1B	0.807	0.120	17	37733029	intron variant	G/A;C	snv			3
rs11263761	HNF1B	1.000	0.080	17	37737784	intron variant	A/G	snv		0.44	2
rs11263763	HNF1B	0.882	0.200	17	37743574	intron variant	A/G	snv		0.43	2
rs757210	HNF1B	0.807	0.160	17	37736525	intron variant	C/G;T	snv			2
rs10908278	HNF1B	0.925	0.160	17	37739961	intron variant	A/C;T	snv			1
rs2005705	HNF1B	0.925	0.120	17	37736310	intron variant	G/A	snv		0.46	1
rs8064454	HNF1B	0.925	0.120	17	37741595	intron variant	C/A;G	snv			1
rs11658063	HNF1B	0.851	0.120	17	37743881	intron variant	G/C;T	snv			1
rs4795218	HNF1B ; LOC105371754	0.925	0.120	17	37718512	intron variant	A/G	snv		0.82	1
rs12951345	HNF1B ; LOC105371754	1.000	0.120	17	37717865	intron variant	C/A	snv		0.80	1
rs17138478	HNF1B ; LOC105371754			17	37713312	intron variant	C/A;T	snv		0.11	1
rs3110641	HNF1B ; LOC105371755			17	37687414	intron variant	G/A	snv		0.32	1
rs11649743	LOC105371754 ; HNF1B	0.925	0.080	17	37714971	intron variant	A/G	snv		0.85	1