DisGeNET - a database of gene-disease associations

List of shared variants

mathematical ability, C0596887

Disease: Body mass index

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
rs2239647	AKAP6	0.851	0.080	14	32823537	synonymous variant	A/C	snv	0.60	0.65	7
rs613872	TCF4	0.851	0.120	18	55543071	intron variant	G/T	snv		0.88	6
rs1167827	HIP1			7	75533848	3 prime UTR variant	G/A	snv		0.37	5
rs6870983	TMEM161B-AS1			5	88401716	intron variant	C/T	snv		0.29	3
rs10858334	OLFM1			9	135097939	3 prime UTR variant	C/A;G	snv		9.4E-02	2
rs10954772	PURG			8	31006422	intron variant	T/A;C	snv			2
rs1492014				3	94352637	intergenic variant	T/C;G	snv			2
rs2837992	BACE2			21	41248593	intron variant	T/C	snv		0.64	2
rs6575340	UNC79			14	93557626	intron variant	G/A	snv		0.61	2
rs7749708	RGS17			6	153054772	intron variant	C/T	snv		0.39	2
rs8024137	DPH6 ; DPH6-DT			15	35545096	intron variant	A/T	snv		0.88	2