DisGeNET - a database of gene-disease associations

List of shared variants

Pediatric Obesity, C2362324

Disease: Essential Hypertension

Source: ALL

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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
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
rs1137101	LEPR	0.554	0.760	1	65592830	missense variant	A/G	snv	0.51	0.50	77
rs4994	ADRB3	0.578	0.640	8	37966280	missense variant	A/G	snv	0.11	9.2E-02	65
rs659366	UCP2	0.724	0.520	11	73983709	non coding transcript exon variant	C/T	snv		0.40	17
rs3918188	NOS3	0.776	0.280	7	151005693	intron variant	C/A;T	snv			10
rs743506	NOS3	0.925	0.120	7	151009827	intron variant	G/A;C	snv			4