DisGeNET - a database of gene-disease associations

List of shared variants

Serum total cholesterol measurement, C1445957

Disease: White Blood Cell Count procedure

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
rs1800961	HNF4A	0.851	0.160	20	44413724	missense variant	C/T	snv	3.1E-02	2.5E-02	17
rs635634		0.882	0.160	9	133279427	upstream gene variant	T/A;C	snv			17
rs2519093	ABO	0.882	0.200	9	133266456	intron variant	T/C	snv			14
rs2954021		1.000	0.040	8	125469835	intron variant	A/G	snv		0.54	13
rs445	CDK6			7	92779056	intron variant	C/T	snv		0.14	9
rs34208856	HBS1L			6	135099930	intron variant	TT/-;T;TTT;TTTTTTTTT	delins			6
rs55709272	IL1RN			2	113109711	intron variant	T/A;C	snv			5
rs6734238		1.000	0.080	2	113083453	upstream gene variant	A/G	snv		0.39	5
rs13135092	SLC39A8			4	102276925	intron variant	A/G	snv		5.1E-02	4