DisGeNET - a database of gene-disease associations

List of shared variants

Corpuscular Hemoglobin Concentration Mean, C4528257

Disease: Diastolic blood pressure

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
rs1799945	LOC108783645 ; HFE	0.452	0.760	6	26090951	missense variant	C/G;T	snv	0.11	0.10	226
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		92
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	47
rs653178	ATXN2	0.672	0.600	12	111569952	intron variant	C/T	snv		0.67	41
rs79105258	CUX2			12	111280427	intron variant	C/A;T	snv			24
rs17696736	NAA25	0.827	0.240	12	112049014	intron variant	A/G	snv		0.30	18
rs687621	ABO	0.851	0.240	9	133261662	intron variant	G/A;C	snv			18
rs198851	H4C3			6	26104404	downstream gene variant	T/A;C;G	snv			15
rs10224002	PRKAG2	0.925	0.080	7	151717955	intron variant	A/G	snv		0.31	12
rs9472135	LOC107986598	0.925	0.120	6	43842065	intron variant	T/A;C;G	snv			9
rs11066188	HECTD4	0.851	0.320	12	112172910	intron variant	G/A;C	snv	0.30; 4.1E-06		7
rs17630235	TRAFD1	0.925	0.120	12	112153882	downstream gene variant	G/A;C	snv			7
rs7753826		0.925	0.120	6	26042011	upstream gene variant	T/A;C	snv			6
rs668459				6	139514552	intron variant	C/T	snv		0.51	5
rs5762862	ZNRF3			22	28856744	intergenic variant	G/A;T	snv			4
rs17737768	PRKCE			2	46129994	intron variant	T/C	snv		8.1E-02	2