DisGeNET - a database of gene-disease associations

List of shared variants

Dyslexia, C0476254

Disease: Developmental reading disorder

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
rs2274305	DCDC2	0.925	0.120	6	24290975	missense variant	T/C	snv	0.65	0.51	2
rs4599626	DCDC2	0.925	0.120	6	24341129	intron variant	C/A	snv		0.33	2
rs6456593	DCDC2	0.925	0.120	6	24174101	3 prime UTR variant	C/G	snv		0.34	2
rs6922023	DCDC2	0.925	0.120	6	24347889	intron variant	G/A	snv		0.22	2
rs6935076	KIAA0319	0.925	0.120	6	24644094	intron variant	C/T	snv		0.30	2
rs9313548		0.925	0.120	5	171534296	TF binding site variant	C/T	snv		0.56	2
rs9467075	DCDC2	0.925	0.120	6	24205008	synonymous variant	G/A	snv	0.13	0.14	2