RNF150, ring finger protein 150, 57484

N. diseases: 6; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10007052
rs10007052
Entrez Id: 57484
Gene Symbol: RNF150
RNF150
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		0.710 GeneticVariation BEFREE Our findings indicated that rs10007052 in the RNF150 and rs3733829 in the EGLN2 gene were significantly associated with the risk of COPD in Chinese populations of Hainan province. 25609945 2015
dbSNP: rs10007052
rs10007052
Entrez Id: 57484
Gene Symbol: RNF150
RNF150
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		A 0.710 GeneticVariation GWASCAT Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease. 23144326 2012
dbSNP: rs41337747
rs41337747
Entrez Id: 57484
Gene Symbol: RNF150
RNF150
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs41337747
rs41337747
Entrez Id: 57484
Gene Symbol: RNF150
RNF150
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018