DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Gene: HNF1A-AS1 ×

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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
rs1169288	HNF1A-AS1 ; HNF1A	0.776	0.160	12	120978847	missense variant	A/C;T	snv	0.35		8
rs2244608	HNF1A ; HNF1A-AS1	0.882	0.160	12	120979185	intron variant	A/G	snv		0.29	6
rs7953249	HNF1A-AS1	0.882	0.160	12	120965921	splice region variant	G/A	snv		0.59	4
rs7305618	HNF1A-AS1	0.925	0.160	12	120965129	intron variant	C/T	snv		0.28	2
rs2650000	HNF1A-AS1	0.851	0.200	12	120951159	intron variant	A/C	snv		0.70	2
rs2255531	HNF1A ; HNF1A-AS1			12	120977112	intron variant	G/A	snv		0.35	2
rs1800574	HNF1A ; HNF1A-AS1	0.882	0.080	12	120979061	missense variant	C/T	snv	2.9E-02	2.2E-02	2
rs6489786	HNF1A-AS1			12	120960072	intron variant	A/G	snv		0.70	1
rs77929563	HNF1A-AS1			12	120961699	intron variant	T/A	snv		7.1E-03	1
rs7135337	HNF1A-AS1			12	120966352	intron variant	A/C;T	snv			1
rs2243616	HNF1A-AS1			12	120968567	intron variant	G/T	snv		0.70	1
rs2251468	HNF1A-AS1			12	120967323	intron variant	C/A;G;T	snv			1
rs80019595	HNF1A ; HNF1A-AS1			12	120979503	intron variant	C/G;T	snv			1