DisGeNET - a database of gene-disease associations

Variant: rs10940767 ×

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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

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs10940767

LINC02109

CUI:	C0017168
Disease:	Gastroesophageal reflux disease

Gastroesophageal reflux disease

0.700

GeneticVariation

GWASCAT

Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases.

2019