DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Disease: Body mass index ×

Variants associated to the Gene: NRXN3 ×

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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
rs10150332	NRXN3			14	79470621	intron variant	T/C	snv		0.26	3
rs17109256	NRXN3			14	79473650	intron variant	G/A	snv		0.21	1
rs7141420	NRXN3	1.000	0.080	14	79433111	intron variant	C/T	snv		0.56	1
rs7144011	NRXN3	1.000	0.080	14	79474040	intron variant	G/T	snv		0.21	1