DisGeNET - a database of gene-disease associations

List of shared variants

Corpuscular Hemoglobin Concentration Mean, C4528257

Disease: Intelligence

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
rs10189857	BCL11A	1.000	0.080	2	60486100	intron variant	A/G	snv		0.42	6
rs2032447	H3C3 ; H2BC3 ; H2AC5P	0.925	0.120	6	26044141	non coding transcript exon variant	A/G	snv	4.1E-06; 0.67	0.67	6
rs2071303	LOC108783645 ; HFE	0.882	0.120	6	26091108	splice region variant	T/C	snv	0.38	0.36	6
rs7224296	LRRC37A2 ; NSF	0.882	0.160	17	46722680	intron variant	G/A	snv		0.59	5
rs8067056	MAPT	0.925	0.080	17	46006582	intron variant	T/C;G	snv		0.30	5
rs17563986	MAPT	1.000	0.040	17	45913906	intron variant	A/G	snv		0.14	4
rs2074404	LRRC37A2 ; WNT3	0.925	0.120	17	46788073	intron variant	T/G	snv		0.27	4
rs754593	MAPT	1.000	0.040	17	45977330	non coding transcript exon variant	G/A	snv		0.52	4
rs916888	LRRC37A2 ; WNT3			17	46785767	intron variant	T/C	snv		0.19	4
rs242559	MAPT	1.000	0.080	17	45948522	intron variant	C/A	snv		0.71	3
rs7581162	BCL11A			2	60477349	intron variant	T/A	snv		0.49	3
rs17426174	LINC02210-CRHR1			17	45753572	intron variant	G/C	snv		0.15	2
rs243072	MIR4432HG			2	60391661	intron variant	G/A;C	snv			2
rs243074	MIR4432HG			2	60390626	intron variant	G/A	snv		0.61	2
rs8080583	KANSL1			17	46085231	intron variant	C/A	snv		0.23	2