DisGeNET - a database of gene-disease associations

List of shared variants

Fetal hemoglobin determination, C0200695

Disease: alpha-Thalassemia

Source: ALL

Results per page

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
rs11886868	BCL11A	0.752	0.280	2	60493111	intron variant	C/T	snv		0.65	12
rs4671393	BCL11A	0.790	0.400	2	60493816	intron variant	A/C;G	snv			11
rs1427407	BCL11A	0.827	0.120	2	60490908	intron variant	T/C;G	snv			6