DisGeNET - a database of gene-disease associations

List of shared variants

Uric acid measurement (procedure), C0202239

Disease: Hematocrit procedure

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
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	81
rs780094	GCKR	0.658	0.400	2	27518370	intron variant	T/C	snv		0.67	62
rs334	HBB	0.724	0.240	11	5227002	missense variant	T/A;C;G	snv	3.5E-03		35
rs1800961	HNF4A	0.851	0.160	20	44413724	missense variant	C/T	snv	3.1E-02	2.5E-02	21
rs9895661	BCAS3	0.882	0.200	17	61379228	non coding transcript exon variant	C/T	snv		0.69	10
rs62435145		1.000	0.040	7	1246931	regulatory region variant	G/T	snv		0.51	8
rs760077	MTX1 ; THBS3	0.925	0.120	1	155208991	missense variant	T/A	snv		0.36	8
rs11072567	NRG4			15	76006403	intron variant	A/G	snv		0.43	5