DisGeNET - a database of gene-disease associations

Source: ALL

Variants associated to the Disease: Finding of body mass index ×

Variants associated to the Gene: MTCH2 ×

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
rs3817334	MTCH2	1.000	0.080	11	47629441	intron variant	C/T	snv		0.36	7
rs10838738	MTCH2	1.000	0.080	11	47641497	intron variant	A/G	snv		0.28	6
rs4752856	MTCH2	1.000	0.040	11	47626490	intron variant	G/A	snv		0.28	4