DisGeNET - a database of gene-disease associations

List of shared variants

Myopia, C0027092

Disease: Severe myopia

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
rs3026393	ELP4 ; PAX6	0.925	0.040	11	31790667	intron variant	A/C;G;T	snv	0.48; 8.0E-06; 7.6E-05		2
rs339501	FGF10	0.925	0.040	5	44365531	intron variant	C/T	snv		0.94	2
rs3741834	LUM	0.925	0.040	12	91111607	upstream gene variant	G/A	snv		2.6E-02	2
rs3759223	LUM	0.925	0.040	12	91113006	upstream gene variant	A/G	snv		2.7E-02	2
rs747797174	GOLGA6A	0.925	0.040	15	74070978	missense variant	C/A;G;T	snv	1.2E-05		2
rs79002828	FGF10	0.925	0.040	5	44318015	intron variant	A/G	snv		9.6E-03	2