DisGeNET - a database of gene-disease associations

List of shared variants

Corpuscular Hemoglobin Concentration Mean, C4528257

Disease: Monocyte count 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
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
rs687621	ABO	0.851	0.240	9	133261662	intron variant	G/A;C	snv			18
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
rs7776054	HBS1L			6	135097778	intron variant	A/G	snv		0.24	13
rs9917425	OTOR			20	16755400	intron variant	G/T	snv		0.16	13
rs11611647				12	4224753	intergenic variant	T/C	snv		0.22	4
rs7578982	ACOXL ; MIR4435-2HG			2	111078961	intron variant	T/C	snv		0.27	4