NUP210, nucleoporin 210, 23225

N. diseases: 14; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1048620
rs1048620
Entrez Id: 23225
Gene Symbol: NUP210
NUP210
CUI: C1305855
Disease:
Body mass index
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3796320
rs3796320
Entrez Id: 23225
Gene Symbol: NUP210
NUP210
CUI: C0596887
Disease:
mathematical ability
A 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: rs73018809
rs73018809
Entrez Id: 23225
Gene Symbol: NUP210
NUP210
CUI: C1956346
Disease:
Coronary Artery Disease
T 0.700 GeneticVariation GWASCAT Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes. 29695241 2018
dbSNP: rs73018809
rs73018809
Entrez Id: 23225
Gene Symbol: NUP210
NUP210
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
T 0.700 GeneticVariation GWASCAT Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes. 29695241 2018
dbSNP: rs9845966
rs9845966
Entrez Id: 23225
Gene Symbol: NUP210
NUP210
CUI: C1305855
Disease:
Body mass index
T 0.700 GeneticVariation GWASCAT The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. 26426971 2015
dbSNP: rs17038082
rs17038082
Entrez Id: 23225
Gene Symbol: NUP210
NUP210
CUI: C0027051
Disease:
Myocardial Infarction
0.700 GeneticVariation GWASDB Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. 21211798 2011
dbSNP: rs354476
rs354476
Entrez Id: 23225
Gene Symbol: NUP210
NUP210
CUI: C0014175
Disease:
Endometriosis
0.010 GeneticVariation BEFREE Immunohistofluorescence analysis for assessing whether GP210 is expressed in endometrial tissues from patients and controls; genotyping and case-control study for assessing the association between rs354476 within NUP210 and risk of endometriosis; in vitro luciferase assay for assessing the functional activity of rs354476. 31256999 2019
dbSNP: rs354476
rs354476
Entrez Id: 23225
Gene Symbol: NUP210
NUP210
CUI: C0009402
Disease:
Colorectal Carcinoma
0.010 GeneticVariation BEFREE Statistically significant associations were found between the risk of CRC and the variant alleles of KIAA0182 (rs709805) (odds ratio = 1.57; 95% confidence interval = 1.06-2.78, for the variant homozygotes) and NUP210 genes (rs354476) (odds ratio = 1.36; 95% confidence interval = 1.02-1.82, for the variant homozygotes). 22282400 2012