DisGeNET - a database of gene-disease associations

Source: GWASDB

Variants associated to the Gene: APOB ×

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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
rs1800479	APOB			2	21004511	intron variant	C/G	snv	0.16	0.17	3
rs3749054	APOB			2	21014366	intron variant	A/T	snv		0.13	3
rs12720847	APOB			2	21012503	missense variant	G/A;C	snv	5.1E-03		1
rs3791980	APOB			2	21022457	intron variant	G/T	snv		0.70	1
rs11126598	APOB			2	21017492	intron variant	A/G	snv		0.73	1
rs11680233	APOB			2	21017159	intron variant	A/C;T	snv			1
rs1469513	APOB	1.000	0.080	2	21036690	intron variant	T/C	snv		0.34	1