DisGeNET - a database of gene-disease associations

List of shared variants

Monocyte count procedure, C0200637

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
rs334	HBB	0.724	0.240	11	5227002	missense variant	T/A;C;G	snv	3.5E-03		35
rs7776054	HBS1L			6	135097778	intron variant	A/G	snv		0.24	13