DisGeNET - a database of gene-disease associations

Source: GWASDB

Disease: Barrett Esophagus ×

Variant: rs9936833 ×

Results per page

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

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs9936833

rs9936833

CUI:	C0004763
Disease:	Barrett Esophagus

Barrett Esophagus

C

0.820

GeneticVariation

GWASDB

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.

2012