NUTF2, nuclear transport factor 2, 10204

N. diseases: 11; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2271293
rs2271293
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0392885
Disease:
High density lipoprotein measurement 		0.800 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs2271293
rs2271293
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.800 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906 2009
dbSNP: rs2271293
rs2271293
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0392885
Disease:
High density lipoprotein measurement 		G 0.800 GeneticVariation GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009
dbSNP: rs2271293
rs2271293
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0392885
Disease:
High density lipoprotein measurement 		G 0.800 GeneticVariation GWASCAT Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009
dbSNP: rs2271293
rs2271293
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0392885
Disease:
High density lipoprotein measurement 		A 0.800 GeneticVariation GWASCAT Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906 2009
dbSNP: rs1124324
rs1124324
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0392885
Disease:
High density lipoprotein measurement 		C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs1124324
rs1124324
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs11553287
rs11553287
Entrez Id: 10204;23644
Gene Symbol: NUTF2;EDC4
NUTF2;EDC4
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs2271294
rs2271294
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs7198357
rs7198357
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C4528257
Disease:
Corpuscular Hemoglobin Concentration Mean 		0.700 GeneticVariation GWASDB Seventy-five genetic loci influencing the human red blood cell. 23222517 2012
dbSNP: rs2271293
rs2271293
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0010068
Disease:
Coronary heart disease 		0.700 GeneticVariation GWASDB Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. 21347282 2011
dbSNP: rs2271293
rs2271293
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		A 0.700 GeneticVariation GWASDB Common variants at 30 loci contribute to polygenic dyslipidemia. 19060906 2009
dbSNP: rs2271293
rs2271293
Entrez Id: 10204
Gene Symbol: NUTF2
NUTF2
CUI: C0428472
Disease:
Serum HDL cholesterol measurement 		G 0.700 GeneticVariation GWASDB Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. 19060911 2009