Source: INFERRED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs7937
rs7937
Entrez Id: 53916;100529262;100529264
Gene Symbol: RAB4B;MIA-RAB4B;RAB4B-EGLN2
RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		T 0.830 GeneticVariation GWASCAT Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. 28166215 2017
dbSNP: rs7937
rs7937
Entrez Id: 53916;100529262;100529264
Gene Symbol: RAB4B;MIA-RAB4B;RAB4B-EGLN2
RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.830 GeneticVariation GWASDB Genotyping this single nucleotide polymorphism (SNP) and another nearby SNP in linkage disequilibrium (rs2604894) in 2859 subjects from the family-based International COPD Genetics Network study (ICGN) demonstrated supportive evidence for association for COPD (P = 0.28 and 0.11 for rs7937 and rs2604894), pre-bronchodilator FEV(1) (P = 0.08 and 0.04) and severe (GOLD 3&4) COPD (P = 0.09 and 0.017). 22080838 2012
dbSNP: rs7937
rs7937
Entrez Id: 53916;100529262;100529264
Gene Symbol: RAB4B;MIA-RAB4B;RAB4B-EGLN2
RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.830 GeneticVariation GWASCAT Genotyping this single nucleotide polymorphism (SNP) and another nearby SNP in linkage disequilibrium (rs2604894) in 2859 subjects from the family-based International COPD Genetics Network study (ICGN) demonstrated supportive evidence for association for COPD (P = 0.28 and 0.11 for rs7937 and rs2604894), pre-bronchodilator FEV(1) (P = 0.08 and 0.04) and severe (GOLD 3&4) COPD (P = 0.09 and 0.017). 22080838 2012
dbSNP: rs2233152
rs2233152
Entrez Id: 8190;100529262
Gene Symbol: MIA;MIA-RAB4B
MIA;MIA-RAB4B
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		A 0.800 GeneticVariation GWASCAT A genome-wide association study identifies three new risk loci for Kawasaki disease. 22446962 2012
dbSNP: rs2233152
rs2233152
Entrez Id: 8190;100529262
Gene Symbol: MIA;MIA-RAB4B
MIA;MIA-RAB4B
CUI: C0026691
Disease:
Mucocutaneous Lymph Node Syndrome 		A 0.800 GeneticVariation GWASDB A genome-wide association study identifies three new risk loci for Kawasaki disease. 22446962 2012
dbSNP: rs2604909
rs2604909
Entrez Id: 53916;100529262;100529264
Gene Symbol: RAB4B;MIA-RAB4B;RAB4B-EGLN2
RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C0200638
Disease:
Eosinophil count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17726276
rs17726276
Entrez Id: 53916;100529262;100529264
Gene Symbol: RAB4B;MIA-RAB4B;RAB4B-EGLN2
RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C2985280
Disease:
Blood Protein Measurement 		A 0.700 GeneticVariation GWASCAT Genomic atlas of the human plasma proteome. 29875488 2018
dbSNP: rs2233154
rs2233154
Entrez Id: 8190;100529262
Gene Symbol: MIA;MIA-RAB4B
MIA;MIA-RAB4B
CUI: C2985280
Disease:
Blood Protein Measurement 		C 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs7937
rs7937
Entrez Id: 53916;100529262;100529264
Gene Symbol: RAB4B;MIA-RAB4B;RAB4B-EGLN2
RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs7937
rs7937
Entrez Id: 53916;100529262;100529264
Gene Symbol: RAB4B;MIA-RAB4B;RAB4B-EGLN2
RAB4B;MIA-RAB4B;RAB4B-EGLN2
CUI: C1519383
Disease:
Smoking Behaviors 		0.700 GeneticVariation GWASDB Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. 20418888 2010