Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0003873
Disease:
Rheumatoid Arthritis
A 0.800 GeneticVariation GWASCAT Genetic influences on susceptibility to rheumatoid arthritis in African-Americans. 30423114 2019
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.800 GeneticVariation GWASCAT Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis. 26546613 2016
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0003873
Disease:
Rheumatoid Arthritis
A 0.800 GeneticVariation GWASCAT High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. 24532676 2015
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0003873
Disease:
Rheumatoid Arthritis
A 0.800 GeneticVariation GWASCAT Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342 2014
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0003873
Disease:
Rheumatoid Arthritis
A 0.800 GeneticVariation GWASDB Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342 2014
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
G 0.800 GeneticVariation GWASDB Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. 18978792 2008
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
G 0.800 GeneticVariation GWASCAT Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. 18978792 2008
dbSNP: rs4750316
rs4750316
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.710 GeneticVariation GWASDB High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596 2012
dbSNP: rs4750316
rs4750316
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0003873
Disease:
Rheumatoid Arthritis
0.710 GeneticVariation BEFREE Here we show that three of these SNPs, mapping to chromosome 10p15 (rs4750316), 12q13 (rs1678542) and 22q13 (rs3218253), are also associated (trend P = 4 x 10(-5), P = 4 x 10(-4) and P = 4 x 10(-4), respectively) in a validation study of 4,106 individuals with rheumatoid arthritis and an expanded reference group of 11,238 subjects, confirming them as true susceptibility loci in individuals of European ancestry. 18794857 2008
dbSNP: rs2181622
rs2181622
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0004364
Disease:
Autoimmune Diseases
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2181622
rs2181622
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2181622
rs2181622
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2181622
rs2181622
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0007570
Disease:
Celiac Disease
0.700 GeneticVariation GWASCAT Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis. 26546613 2016
dbSNP: rs4750316
rs4750316
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0004364
Disease:
Autoimmune Diseases
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. 21383967 2011
dbSNP: rs4750316
rs4750316
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0021053
Disease:
Immune System Diseases
0.700 GeneticVariation GWASDB Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. 21383967 2011
dbSNP: rs4750316
rs4750316
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0026769
Disease:
Multiple Sclerosis
0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364 2011
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0026769
Disease:
Multiple Sclerosis
0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. 22190364 2011
dbSNP: rs4750316
rs4750316
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C3495559
Disease:
Juvenile arthritis
0.010 GeneticVariation BEFREE In the present study, we analyzed three single nucleotide polymorphisms (SNPs), namely PTPRC (rs10919563), TYK2 (rs34536443) and PRKCQ (rs4750316), which were found to be associated with JIA in previous studies. 28990043 2017
dbSNP: rs947474
rs947474
Entrez Id: 399715;399716
Gene Symbol: LINC02649;LINC02656
LINC02649;LINC02656
CUI: C0004943
Disease:
Behcet Syndrome
0.010 GeneticVariation BEFREE No statistically significant differences in the frequencies of rs702873, rs13031237, rs4750316, rs11258747, and rs947474 between BD patients and controls were observed. 26784953 2016