DisGeNET - a database of gene-disease associations

List of shared variants

mathematical ability, C0596887

Disease: Body Height

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
rs13107325	SLC39A8	0.776	0.520	4	102267552	missense variant	C/A;T	snv	4.0E-06; 4.5E-02		34
rs34811474	ANAPC4	1.000	0.040	4	25407216	missense variant	G/A;T	snv	0.15; 4.1E-06		8
rs10189857	BCL11A	1.000	0.080	2	60486100	intron variant	A/G	snv		0.42	6
rs1167827	HIP1			7	75533848	3 prime UTR variant	G/A	snv		0.37	5
rs2093210	C14orf39	1.000	0.040	14	60490561	intron variant	C/T	snv		0.45	4
rs11545169	PSMD2			3	184302754	missense variant	G/T	snv	0.13	0.11	3
rs8067165	LOC105376799			17	8128618	upstream gene variant	C/A;G;T	snv			3
rs9217	ZBTB4	1.000	0.080	17	7459769	3 prime UTR variant	T/A;C	snv			3
rs191903670	PFKFB4			3	48540620	intron variant	A/T	snv		1.1E-02	2
rs2425848	CDH22			20	46279305	intron variant	A/C;G	snv			2
rs7175692	SNORD13E ; DENND4A			15	65698258	intron variant	A/G	snv		0.27	2
rs72766638	BRD3			9	134066656	intron variant	C/A;T	snv			2