DisGeNET - a database of gene-disease associations

rs80358192, COL8A2

N. diseases: 6

Disease: Corneal dystrophy ×

Source: ALL

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Corneal dystrophy

CUI:	C0010036
Disease:	Corneal dystrophy

0.010

GeneticVariation

BEFREE

Distinct Clinical Phenotype of Corneal Dystrophy Predicts the p.(Leu450Trp) Substitution in COL8A2.

2016