Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2242285
rs2242285
Entrez Id: 26018;115286
Gene Symbol: LRIG1;SLC25A26
LRIG1;SLC25A26
CUI: C0018803
Disease:
Heart Function Tests
A 0.700 GeneticVariation GWASCAT Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. 21076409 2010
dbSNP: rs13078828
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: rs9827908
rs9827908
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0442874
Disease:
Neuropathy
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: rs9827908
rs9827908
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY 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: rs9827908
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: rs9827908
rs9827908
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C1836231
Disease:
HIV-1, RESISTANCE 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: rs9827908
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
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0009404
Disease:
Colorectal Neoplasms
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs812481
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0009402
Disease:
Colorectal Carcinoma
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs812481
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C1837315
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs812481
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0346629
Disease:
Malignant neoplasm of large intestine
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs812481
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C2677123
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs812481
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0007102
Disease:
Malignant tumor of colon
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs812481
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C3554460
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs812481
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C1319315
Disease:
Adenocarcinoma of large intestine
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs812481
rs812481
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C2675481
Disease:
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
G 0.700 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821 2015
dbSNP: rs2242285
rs2242285
Entrez Id: 26018;115286
Gene Symbol: LRIG1;SLC25A26
LRIG1;SLC25A26
CUI: C0429097
Disease:
QRS complex feature
0.700 GeneticVariation GWASCAT 52 Genetic Loci Influencing Myocardial Mass. 27659466 2016
dbSNP: rs6147862
rs6147862
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6147862
rs6147862
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0524587
Disease:
Mean Corpuscular Volume (result)
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs11706832
rs11706832
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0017638
Disease:
Glioma
C 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
dbSNP: rs11706832
rs11706832
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0085136
Disease:
Central Nervous System Neoplasms
C 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: rs17831815
rs17831815
Entrez Id: 26018;115286
Gene Symbol: LRIG1;SLC25A26
LRIG1;SLC25A26
CUI: C0871470
Disease:
Systolic Pressure
T 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs11706832
rs11706832
Entrez Id: 26018
Gene Symbol: LRIG1
LRIG1
CUI: C0017638
Disease:
Glioma
0.710 GeneticVariation BEFREE Thus, for the first time, changes in physiological Lrig1 expression have been linked to gliomagenesis, whereby the SNP rs11706832 may affect glioma risk by regulating LRIG1 expression. 29391393 2018
dbSNP: rs147372871
rs147372871
Entrez Id: 26018;115286
Gene Symbol: LRIG1;SLC25A26
LRIG1;SLC25A26
CUI: C0022661
Disease:
Kidney Failure, Chronic
0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs202007714
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