CD80, CD80 molecule, 941

N. diseases: 233; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6804441
rs6804441
Entrez Id: 941
Gene Symbol: CD80
CD80
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.810 GeneticVariation BEFREE Single nuclear polymorphism rs2222631 was found associated with SLE with genome-wide significance (P_all=4.5E-08, OR=0.86) and is independent of rs6804441 in CD80, whose association was reported previously. 25862617 2016
dbSNP: rs6804441
rs6804441
Entrez Id: 941
Gene Symbol: CD80
CD80
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
A 0.810 GeneticVariation GWASCAT Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568 2013
dbSNP: rs6804441
rs6804441
Entrez Id: 941
Gene Symbol: CD80
CD80
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
A 0.810 GeneticVariation GWASDB Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568 2013
dbSNP: rs2222631
rs2222631
Entrez Id: 941
Gene Symbol: CD80
CD80
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.710 GeneticVariation BEFREE Interaction of CD80 (rs2222631</span>) and ALOX5AP (rs12876893) was found to be significantly associated with SLE (OR_int=1.16, P_int_all=7.7E-04 at false discovery rate<0.05). 25862617 2016
dbSNP: rs2222631
rs2222631
Entrez Id: 941
Gene Symbol: CD80
CD80
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.710 GeneticVariation GWASCAT Single nuclear polymorphism rs2222631 was found associated with SLE with genome-wide significance (P_all=4.5E-08, OR=0.86) and is independent of rs6804441 in CD80, whose association was reported previously. 25862617 2016
dbSNP: rs1599795
rs1599795
Entrez Id: 941;51300
Gene Symbol: CD80;TIMMDC1
CD80;TIMMDC1
CUI: C0020676
Disease:
Hypothyroidism
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7628626
rs7628626
Entrez Id: 941;51300
Gene Symbol: CD80;TIMMDC1
CD80;TIMMDC1
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE However, <i>ICOS</i> rs4404254 T>C, CD28 rs3116496 T>C and CD80 rs7628626 C>A SNPs were not associated with the risk of HCC. 31235485 2019
dbSNP: rs7628626
rs7628626
Entrez Id: 941;51300
Gene Symbol: CD80;TIMMDC1
CD80;TIMMDC1
CUI: C0686619
Disease:
Secondary malignant neoplasm of lymph node
0.010 GeneticVariation BEFREE CD80-rs7628626-GT was apparently less in the patients with lymph node metastasis (p=0.004) or in advanced stage (p=0.037). 25497975 2015
dbSNP: rs1599795
rs1599795
Entrez Id: 941;51300
Gene Symbol: CD80;TIMMDC1
CD80;TIMMDC1
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE Our findings have shown that the SNP rs1599795 in CD80 3'-UTR, through disrupting the regulatory role of miR-132-3p, miR-212-3p, and miR-361-5p in CD80 expression, contributed to the occurrence of gastric cancer. 24981235 2014
dbSNP: rs1599795
rs1599795
Entrez Id: 941;51300
Gene Symbol: CD80;TIMMDC1
CD80;TIMMDC1
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.010 GeneticVariation BEFREE Our findings have shown that the SNP rs1599795 in CD80 3'-UTR, through disrupting the regulatory role of miR-132-3p, miR-212-3p, and miR-361-5p in CD80 expression, contributed to the occurrence of gastric cancer. 24981235 2014
dbSNP: rs13071247
rs13071247
Entrez Id: 941
Gene Symbol: CD80
CD80
CUI: C0027651
Disease:
Neoplasms
0.010 GeneticVariation BEFREE Fo0r the latter, correlative data support a CD80 rs13071247 genotype association with CD80 tumor RNA expression (p=0.006). 23382860 2013