DisGeNET - a database of gene-disease associations

List of shared variants

Lymphocyte Count measurement, C0200635

Disease: Corpuscular Hemoglobin Concentration Mean

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
rs4737010	ANK1			8	41772929	intron variant	G/A	snv		0.32	6
rs142550358				9	88777772	intron variant	CT/-	delins		3.9E-02	5
rs9494142	LOC105378010			6	135110502	TF binding site variant	T/C	snv		0.21	5
rs9272219	HLA-DQA1	0.925	0.160	6	32634492	intron variant	G/T	snv		0.29	4
rs2157691	SPTA1			1	158613048	intron variant	G/C	snv		0.24	3
rs422112	LINC02210-CRHR1 ; LINC02210	1.000	0.080	17	45650771	non coding transcript exon variant	G/A	snv		0.14	3
rs17157836	LOC105378286 ; MARCHF8			10	45468138	intron variant	T/C	snv		6.3E-02	2
rs2524035				6	29864555	intron variant	A/G	snv		0.81	2
rs34664882	ANK1			8	41686157	missense variant	G/A	snv	2.3E-02	2.1E-02	2
rs9379851				6	26354552	regulatory region variant	A/C	snv		7.6E-02	2