DisGeNET - a database of gene-disease associations

List of shared variants

Multiple Chronic Conditions, C3266262

Disease: Cardiovascular Diseases

Source: ALL

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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
rs1800562	LOC108783645 ; HFE	0.435	0.880	6	26092913	missense variant	G/A	snv	3.3E-02	3.8E-02	262
rs1799983	NOS3	0.430	0.880	7	150999023	missense variant	T/A;G	snv	0.75		246
rs1799945	LOC108783645 ; HFE	0.452	0.760	6	26090951	missense variant	C/G;T	snv	0.11	0.10	226
rs2043211	CARD8	0.653	0.480	19	48234449	missense variant	A/T	snv	0.33	0.29	29
rs10846744	SCARB1	0.763	0.160	12	124827879	intron variant	G/C	snv		0.32	11
rs11571836	BRCA2	0.827	0.200	13	32399302	3 prime UTR variant	A/G;T	snv			6
rs1799943	BRCA2	0.925	0.080	13	32316435	5 prime UTR variant	G/A;C;T	snv	0.25		5
rs16928751	ADIPOR2	0.925	0.120	12	1781033	synonymous variant	G/A	snv	0.11	0.14	3
rs1058322	ADIPOR2	1.000	0.040	12	1727813	intron variant	C/T	snv		0.30	2
rs11061937	ADIPOR2	1.000	0.040	12	1707447	intron variant	T/C	snv		0.31	2