NUP210L, nucleoporin 210 like, 91181

N. diseases: 7; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12130660
rs12130660
Entrez Id: 91181
Gene Symbol: NUP210L
NUP210L
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs111804060
rs111804060
Entrez Id: 91181
Gene Symbol: NUP210L
NUP210L
CUI: C1278049
Disease:
Serum gamma-glutamyl transferase measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs2494668
rs2494668
Entrez Id: 91181
Gene Symbol: NUP210L
NUP210L
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: rs4845360
rs4845360
Entrez Id: 91181
Gene Symbol: NUP210L
NUP210L
CUI: C2985280
Disease:
Blood Protein Measurement 		G 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs6671009
rs6671009
Entrez Id: 91181
Gene Symbol: NUP210L
NUP210L
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: rs6671166
rs6671166
Entrez Id: 91181
Gene Symbol: NUP210L
NUP210L
CUI: C0202236
Disease:
Triglycerides measurement 		G 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs2494663
rs2494663
Entrez Id: 91181
Gene Symbol: NUP210L
NUP210L
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		A 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4400599
rs4400599
Entrez Id: 91181
Gene Symbol: NUP210L
NUP210L
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016