DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Hypertensive disease ×

Variants associated to the Gene: PPARG ×

Results per page

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
rs1801282	PPARG	0.500	0.840	3	12351626	missense variant	C/G	snv	0.11	8.9E-02	131
rs1805192	PPARG	0.510	0.840	3	12379739	missense variant	C/G	snv			121
rs3856806	PPARG	0.637	0.440	3	12434058	synonymous variant	C/T	snv	0.13	0.11	41
rs121909244	PPARG	0.776	0.160	3	12434111	missense variant	C/A;T	snv	4.0E-06		11
rs1175543	PPARG	0.851	0.120	3	12424934	intron variant	A/G	snv		0.28	5
rs2972164	PPARG	0.925	0.080	3	12292917	intron variant	T/C	snv		0.46	3
rs9817428	PPARG	0.925	0.120	3	12298768	intron variant	C/A	snv		0.31	3
rs12633551	PPARG			3	12318995	intron variant	C/T	snv		2.8E-02	2
rs12631819	PPARG			3	12301362	intron variant	G/A;T	snv			1
rs6802898	PPARG			3	12349708	intron variant	C/T	snv		0.27	1