DisGeNET - a database of gene-disease associations

List of shared variants

Eosinophil count procedure, C0200638

Disease: Celiac Disease

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
rs2476601	AP4B1-AS1 ; PTPN22	0.498	0.800	1	113834946	missense variant	A/G	snv	0.93	0.93	121
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
rs4676410	GPR35	0.716	0.240	2	240624322	intron variant	G/A	snv		0.26	17
rs62324212	IL21-AS1	0.724	0.240	4	122639784	intron variant	C/A;G	snv			15
rs9979383	RUNX1	0.925	0.200	21	35343463	intron variant	C/G;T	snv			5
rs76830965	IL12A-AS1	0.925	0.120	3	159919889	intron variant	C/A;G;T	snv			3