DisGeNET - a database of gene-disease associations

LRIG1, leucine rich repeats and immunoglobulin like domains 1, 26018

N. diseases: 83; N. variants: 13

Disease: Atrial Fibrillation ×

Variant: rs2306272 ×

Source: ALL

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:

rs2306272

rs2306272

Entrez Id:	26018;115286
Gene Symbol:	LRIG1;SLC25A26

LRIG1;SLC25A26

CUI:	C0004238
Disease:

Atrial Fibrillation

C

0.700

GeneticVariation

GWASCAT

Multi-ethnic genome-wide association study for atrial fibrillation.

2018