CD82, CD82 molecule, 3732

N. diseases: 172; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs934178
rs934178
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs934178
rs934178
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs113104107
rs113104107
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C0427460
Disease:
Red cell distribution width determination 		C 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
dbSNP: rs113104107
rs113104107
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		C 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
dbSNP: rs60865046
rs60865046
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs60865046
rs60865046
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C0427460
Disease:
Red cell distribution width determination 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs2303861
rs2303861
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C0400966
Disease:
Non-alcoholic Fatty Liver Disease 		0.010 GeneticVariation BEFREE When Bonferroni correction was applied, NAFLD was significantly associated with rs2303861, a variant located in the CD82 gene (P=2.49×10-7, adjusted P=0.0059). 31483122 2019
dbSNP: rs1451539938
rs1451539938
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C0007103
Disease:
Malignant neoplasm of endometrium 		0.010 GeneticVariation BEFREE To investigate the DN effect on tumor migration and invasion, we generated cells that stably co-expressed wild-type (wt) and R273H DN mutant TP53 (273H cells), and wt and R213Q recessive mutant TP53 (213Q cells), by transfection in endometrial cancer cells HHUA that expressed wt p53. 17636407 2007
dbSNP: rs1451539938
rs1451539938
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C1269955
Disease:
Tumor Cell Invasion 		0.010 GeneticVariation BEFREE To investigate the DN effect on tumor migration and invasion, we generated cells that stably co-expressed wild-type (wt) and R273H DN mutant TP53 (273H cells), and wt and R213Q recessive mutant TP53 (213Q cells), by transfection in endometrial cancer cells HHUA that expressed wt p53. 17636407 2007
dbSNP: rs1451539938
rs1451539938
Entrez Id: 3732
Gene Symbol: CD82
CD82
CUI: C0476089
Disease:
Endometrial Carcinoma 		0.010 GeneticVariation BEFREE To investigate the DN effect on tumor migration and invasion, we generated cells that stably co-expressed wild-type (wt) and R273H DN mutant TP53 (273H cells), and wt and R213Q recessive mutant TP53 (213Q cells), by transfection in endometrial cancer cells HHUA that expressed wt p53. 17636407 2007