DisGeNET - a database of gene-disease associations

List of shared variants

Severe myopia, C0271183

Disease: Myopia, Degenerative

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
rs13382811	ZEB2	0.882	0.040	2	144466053	intron variant	C/T	snv		0.21	4
rs4373767		0.882	0.040	1	219586340	regulatory region variant	C/T	snv		0.32	4
rs7839488	SNTB1	0.882	0.040	8	120550178	intron variant	G/A	snv		0.47	4
rs10034228		0.882	0.040	4	111690594	intergenic variant	T/C	snv		0.32	3
rs577948	MIR100HG	0.882	0.040	11	122159482	intron variant	A/G	snv		0.33	3
rs6469937	SNTB1	0.882	0.040	8	120598198	intron variant	G/A	snv		0.48	3
rs9318086	MIPEP	0.882	0.040	13	23858328	intron variant	A/G	snv		0.55	3
rs2089760	LAMA1	0.925	0.040	18	7118956	upstream gene variant	C/T	snv		0.43	2