DisGeNET - a database of gene-disease associations

List of shared variants

Corpuscular Hemoglobin Concentration Mean, C4528257

Disease: Blood basophil count (lab test)

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
rs3184504	SH2B3 ; ATXN2	0.572	0.600	12	111446804	missense variant	T/A;C;G	snv	0.67		92
rs653178	ATXN2	0.672	0.600	12	111569952	intron variant	C/T	snv		0.67	41
rs334	HBB	0.724	0.240	11	5227002	missense variant	T/A;C;G	snv	3.5E-03		35
rs13331259	FAM234A			16	249924	intron variant	A/G	snv		3.0E-02	14
rs112505971	ANKRD26			10	27068541	intron variant	A/C;G	snv			13
rs2853961				6	31264212	downstream gene variant	G/A	snv		0.38	13
rs3123543	ATF3			1	212617344	intron variant	T/A;C	snv			13
rs3840870	COL1A1			17	50184820	3 prime UTR variant	-/CTTG	delins			13
rs4837892	TTLL11			9	121826025	intron variant	G/T	snv		0.36	13
rs7296503	PDZRN4			12	41306962	intron variant	C/T	snv		0.57	13
rs76792961	FAM234A			16	243594	intron variant	C/T	snv		7.3E-03	13
rs9917425	OTOR			20	16755400	intron variant	G/T	snv		0.16	13
rs218265				4	54542832	intergenic variant	T/C	snv		0.21	10
rs9400271	CCDC162P			6	109286353	non coding transcript exon variant	G/A	snv		0.51	6
rs6920211	LOC105378010			6	135110180	regulatory region variant	T/C	snv		0.29	4
rs1036332	LINC01221			1	199043349	intron variant	A/C	snv		0.70	3
rs9320282	CCDC162P			6	109298174	intron variant	A/G	snv		0.63	2