NCOA2, nuclear receptor coactivator 2, 10499

N. diseases: 95; N. variants: 8
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs57994514
rs57994514
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435 2019
dbSNP: rs10091910
rs10091910
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0201850
Disease:
Alkaline phosphatase measurement 		0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs10504474
rs10504474
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0392885
Disease:
High density lipoprotein measurement 		G 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs10504474
rs10504474
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs113654977
rs113654977
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs76718417
rs76718417
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566 2018
dbSNP: rs16936870
rs16936870
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0429028
Disease:
QT interval feature (observable entity) 		A 0.700 GeneticVariation GWASCAT Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. 24952745 2014
dbSNP: rs13260060
rs13260060
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0026769
Disease:
Multiple Sclerosis 		A 0.700 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602 2013
dbSNP: rs10504473
rs10504473
Entrez Id: 10499
Gene Symbol: NCOA2
NCOA2
CUI: C0028754
Disease:
Obesity 		0.010 GeneticVariation BEFREE Our study suggests a possible association between NCOA2 rs10504473 polymorphism and obesity, and this SNP may influence the susceptibility of obesity in the Chinese Han population. 26261634 2015