DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: BRAP ×

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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
rs3782886	BRAP	0.724	0.480	12	111672685	synonymous variant	T/C	snv	1.9E-02	5.9E-03	7
rs11066001	BRAP	0.763	0.360	12	111681367	intron variant	T/C	snv		5.8E-03	2
rs7136874	BRAP			12	111675854	intron variant	C/T	snv		0.36	1
rs7977828	BRAP			12	111656962	intron variant	A/G	snv		0.27	1
rs10744773	BRAP			12	111649006	intron variant	C/A	snv		0.36	1
rs847895	BRAP			12	111680772	intron variant	T/C	snv		0.18	1
rs3742001	BRAP			12	111665344	intron variant	C/G;T	snv			1