NOL4L, nucleolar protein 4 like, 140688

N. diseases: 16; N. variants: 15
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs159058
rs159058
Entrez Id: 140688;101929698
Gene Symbol: NOL4L;LOC101929698
NOL4L;LOC101929698
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1868385
rs1868385
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1868385
rs1868385
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
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: rs55731315
rs55731315
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs6119897
rs6119897
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. 30643258 2019
dbSNP: rs1555132
rs1555132
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0018681
Disease:
Headache 		A 0.700 GeneticVariation GWASCAT A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N=223,773). 29397368 2018
dbSNP: rs1737889
rs1737889
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0016529
Disease:
Forced expiratory volume function 		T 0.700 GeneticVariation GWASCAT Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. 30061609 2018
dbSNP: rs1742982
rs1742982
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0406208
Disease:
Suntan 		T 0.700 GeneticVariation GWASCAT Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. 29739929 2018
dbSNP: rs6119267
rs6119267
Entrez Id: 140688;149950
Gene Symbol: NOL4L;NOL4L-DT
NOL4L;NOL4L-DT
CUI: C0596887
Disease:
mathematical ability 		C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs875519
rs875519
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs1737890
rs1737890
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		T 0.700 GeneticVariation GWASCAT Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. 28166215 2017
dbSNP: rs910889
rs910889
Entrez Id: 140688;101929698
Gene Symbol: NOL4L;LOC101929698
NOL4L;LOC101929698
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: rs910889
rs910889
Entrez Id: 140688;101929698
Gene Symbol: NOL4L;LOC101929698
NOL4L;LOC101929698
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: rs1555133
rs1555133
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0200637
Disease:
Monocyte count procedure 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1555133
rs1555133
Entrez Id: 140688
Gene Symbol: NOL4L
NOL4L
CUI: C0750880
Disease:
Monocyte count result 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs159058
rs159058
Entrez Id: 140688;101929698
Gene Symbol: NOL4L;LOC101929698
NOL4L;LOC101929698
CUI: C0524587
Disease:
Mean Corpuscular Volume (result) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs159058
rs159058
Entrez Id: 140688;101929698
Gene Symbol: NOL4L;LOC101929698
NOL4L;LOC101929698
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs159058
rs159058
Entrez Id: 140688;101929698
Gene Symbol: NOL4L;LOC101929698
NOL4L;LOC101929698
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs5841107
rs5841107
Entrez Id: 140688;105372592
Gene Symbol: NOL4L;LOC105372592
NOL4L;LOC105372592
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6119267
rs6119267
Entrez Id: 140688;149950
Gene Symbol: NOL4L;NOL4L-DT
NOL4L;NOL4L-DT
CUI: C0427460
Disease:
Red cell distribution width determination 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6119267
rs6119267
Entrez Id: 140688;149950
Gene Symbol: NOL4L;NOL4L-DT
NOL4L;NOL4L-DT
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6141743
rs6141743
Entrez Id: 140688;101929698
Gene Symbol: NOL4L;LOC101929698
NOL4L;LOC101929698
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs67696533
rs67696533
Entrez Id: 140688;149950
Gene Symbol: NOL4L;NOL4L-DT
NOL4L;NOL4L-DT
CUI: C0200641
Disease:
Blood basophil count (lab test) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016