DisGeNET - a database of gene-disease associations

Source: GWASCAT

Variants associated to the Disease: Body mass index ×

Variants associated to the Gene: MAP2K5 ×

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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
rs16951275	MAP2K5			15	67784830	intron variant	T/C	snv		0.30	2
rs2241423	MAP2K5	0.882	0.120	15	67794500	intron variant	G/A	snv		0.29	2
rs3784710	MAP2K5			15	67780120	intron variant	T/C	snv		0.30	2
rs4776970	MAP2K5			15	67788548	intron variant	A/T	snv		0.44	2
rs7175517	MAP2K5			15	67785292	intron variant	A/G	snv		0.30	2
rs8025790	MAP2K5			15	67784061	intron variant	G/T	snv		0.30	2
rs11637027	MAP2K5			15	67645417	intron variant	G/T	snv		0.55	1
rs28376010	MAP2K5			15	67771401	intron variant	G/T	snv		0.27	1
rs3865018	MAP2K5			15	67600428	intron variant	C/T	snv		0.24	1