DisGeNET - a database of gene-disease associations

List of shared variants

Venous Thromboembolism, C1861172

Disease: C-reactive protein measurement

Source: GWASDB ×

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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
rs579459		0.752	0.320	9	133278724	upstream gene variant	C/T	snv		0.81	17
rs657152	ABO	0.882	0.200	9	133263862	intron variant	A/C;T	snv			14
rs505922	ABO	0.689	0.520	9	133273813	intron variant	C/T	snv			12
rs651007		0.851	0.160	9	133278431	upstream gene variant	T/A;C	snv			11
rs612169	ABO			9	133268030	intron variant	G/A	snv			10
rs630014	ABO			9	133274306	intron variant	G/A;C	snv			9
rs687289	ABO	1.000	0.120	9	133261703	intron variant	A/G	snv			9
rs687621	ABO	0.851	0.240	9	133261662	intron variant	G/A;C	snv			9
rs495828		0.827	0.200	9	133279294	upstream gene variant	T/G	snv		0.81	8
rs514659	ABO	0.882	0.120	9	133266790	intron variant	C/A;T	snv			8
rs529565	ABO	0.851	0.120	9	133274084	intron variant	C/T	snv			8
rs545971	ABO			9	133267960	intron variant	T/A;C	snv			8
rs649129		1.000	0.080	9	133278860	upstream gene variant	T/C;G	snv			8
rs674302	ABO			9	133271249	intron variant	A/T	snv			8
rs643434	ABO			9	133266942	intron variant	A/G;T	snv			7
rs644234	ABO			9	133266804	intron variant	G/T	snv			7
rs3758348	SURF4			9	133372523	intron variant	G/C	snv		0.13	4