DisGeNET - a database of gene-disease associations

List of shared variants

Triglycerides measurement, C0202236

Disease: Reticulocyte 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
rs1260326	GCKR	0.645	0.600	2	27508073	missense variant	T/C;G	snv	0.63; 4.0E-06	0.68	55
rs964184	ZPR1	0.716	0.440	11	116778201	3 prime UTR variant	G/C	snv		0.82	35
rs7412	APOE	0.641	0.640	19	44908822	missense variant	C/T	snv	6.2E-02	7.9E-02	20
rs998584				6	43790159	downstream gene variant	C/A	snv		0.41	10
rs1128249	COBLL1	1.000	0.080	2	164672114	intron variant	G/C;T	snv			9
rs4665972	SNX17			2	27375230	intron variant	T/C	snv		0.69	8
rs112875651				8	125494452	intron variant	G/A	snv		0.31	7
rs12454712	BCL2	0.925	0.120	18	63178651	intron variant	T/A;C	snv			7
rs11048456	LOC105369705	1.000	0.080	12	26310149	intron variant	C/T	snv		0.62	6
rs11967262				6	43792590	intergenic variant	C/G	snv		0.41	4
rs1694068	ARL15			5	53987800	intron variant	T/A	snv		0.62	4