DisGeNET - a database of gene-disease associations

List of shared variants

Eosinophil count procedure, C0200638

Disease: Body Height

Source: GWASCAT ×

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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		61
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	55
rs445	CDK6			7	92779056	intron variant	C/T	snv		0.14	9
rs11153159	SESN1			6	109055444	intron variant	C/G;T	snv			2
rs13062095				3	101548541	intergenic variant	T/C	snv		0.24	2
rs4253755	PPARA			22	46219479	intron variant	G/A	snv		8.6E-02	2
rs77929895	SETDB2-PHF11 ; PHF11			13	49498293	intron variant	T/C	snv		8.6E-02	2
rs945631	DIPK1A			1	92960610	intron variant	G/A	snv		4.1E-02	2