DisGeNET - a database of gene-disease associations

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

N. diseases: 83; N. variants: 13

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:

rs9827908

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C1836232
Disease:

ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO

0.700

GeneticVariation

GWASCAT

Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384.

24554482

2014

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C1319315
Disease:

Adenocarcinoma of large intestine

0.700

GeneticVariation

GWASCAT

Novel Common Genetic Susceptibility Loci for Colorectal Cancer.

29917119

2019

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C1319315
Disease:

Adenocarcinoma of large intestine

0.700

GeneticVariation

GWASCAT

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

26151821

2015

dbSNP:

rs9827908

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C1836233
Disease:

AIDS, PROGRESSION TO

0.700

GeneticVariation

GWASCAT

Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384.

24554482

2014

dbSNP:

rs13078828

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0201278
Disease:

Antibody measurement (procedure)

0.700

GeneticVariation

GWASCAT

Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.

24324551

2013

dbSNP:

rs2306272

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

LRIG1;SLC25A26

CUI:	C0004238
Disease:

Atrial Fibrillation

0.700

GeneticVariation

GWASCAT

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

29892015

2018

dbSNP:

rs34080181

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0004238
Disease:

Atrial Fibrillation

0.700

GeneticVariation

GWASCAT

Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.

30061737

2018

dbSNP:

rs3965156

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0005612
Disease:

Birth Weight

0.700

GeneticVariation

GWASCAT

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.

31043758

2019

dbSNP:

rs11706832

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0085136
Disease:

Central Nervous System Neoplasms

0.700

GeneticVariation

GWASCAT

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.

28346443

2017

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C1837315
Disease:

COLORECTAL CANCER, SUSCEPTIBILITY TO, 1

0.700

GeneticVariation

GWASCAT

Novel Common Genetic Susceptibility Loci for Colorectal Cancer.

29917119

2019

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C1837315
Disease:

COLORECTAL CANCER, SUSCEPTIBILITY TO, 1

0.700

GeneticVariation

GWASCAT

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

26151821

2015

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C2675481
Disease:

COLORECTAL CANCER, SUSCEPTIBILITY TO, 10

0.700

GeneticVariation

GWASCAT

Novel Common Genetic Susceptibility Loci for Colorectal Cancer.

29917119

2019

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C2675481
Disease:

COLORECTAL CANCER, SUSCEPTIBILITY TO, 10

0.700

GeneticVariation

GWASCAT

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

26151821

2015

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C3554460
Disease:

COLORECTAL CANCER, SUSCEPTIBILITY TO, 12

0.700

GeneticVariation

GWASCAT

Novel Common Genetic Susceptibility Loci for Colorectal Cancer.

29917119

2019

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C3554460
Disease:

COLORECTAL CANCER, SUSCEPTIBILITY TO, 12

0.700

GeneticVariation

GWASCAT

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

26151821

2015

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C2677123
Disease:

COLORECTAL CANCER, SUSCEPTIBILITY TO, 3

0.700

GeneticVariation

GWASCAT

Novel Common Genetic Susceptibility Loci for Colorectal Cancer.

29917119

2019

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C2677123
Disease:

COLORECTAL CANCER, SUSCEPTIBILITY TO, 3

0.700

GeneticVariation

GWASCAT

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

26151821

2015

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

GWASCAT

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

26151821

2015

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

GWASCAT

Novel Common Genetic Susceptibility Loci for Colorectal Cancer.

29917119

2019

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0009404
Disease:

Colorectal Neoplasms

0.700

GeneticVariation

GWASCAT

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.

26151821

2015

dbSNP:

rs812481

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0009404
Disease:

Colorectal Neoplasms

0.700

GeneticVariation

GWASCAT

Novel Common Genetic Susceptibility Loci for Colorectal Cancer.

29917119

2019

dbSNP:

rs202007714

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

LRIG1;SLC25A26

CUI:	C0201976
Disease:

Creatinine measurement, serum (procedure)

0.700

GeneticVariation

GWASCAT

Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population.

29124443

2018

dbSNP:

rs6147862

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C1261502
Disease:

Finding of Mean Corpuscular Hemoglobin

0.700

GeneticVariation

GWASCAT

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.

27863252

2016

dbSNP:

rs6549120

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C1261502
Disease:

Finding of Mean Corpuscular Hemoglobin

0.700

GeneticVariation

GWASCAT

Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

30595370

2019

dbSNP:

rs11706832

Entrez Id:	26018
Gene Symbol:	LRIG1

LRIG1

CUI:	C0017638
Disease:

Glioma

0.710

GeneticVariation

GWASCAT

Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.

28346443

2017