NPNT, nephronectin, 255743

N. diseases: 55; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34712979
rs34712979
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C1518922
Disease:
peak expiratory flow (procedure) 		A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs34712979
rs34712979
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0035242
Disease:
Respiratory Tract Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34712979
rs34712979
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0016529
Disease:
Forced expiratory volume function 		A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs34712979
rs34712979
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0042834
Disease:
Vital capacity 		A 0.700 GeneticVariation GWASCAT New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. 30804560 2019
dbSNP: rs34712979
rs34712979
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0024117
Disease:
Chronic Obstructive Airway Disease 		A 0.700 GeneticVariation GWASCAT Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. 30804561 2019
dbSNP: rs56388530
rs56388530
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs56388530
rs56388530
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs56388530
rs56388530
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0007222
Disease:
Cardiovascular Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs13112725
rs13112725
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs2866784
rs2866784
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs2866784
rs2866784
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117 2018
dbSNP: rs78213340
rs78213340
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C2985280
Disease:
Blood Protein Measurement 		T 0.700 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
dbSNP: rs13112725
rs13112725
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0871470
Disease:
Systolic Pressure 		G 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs13112725
rs13112725
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. 28135244 2017
dbSNP: rs13112725
rs13112725
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0871470
Disease:
Systolic Pressure 		C 0.700 GeneticVariation GWASCAT Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. 28739976 2017
dbSNP: rs13112725
rs13112725
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0428883
Disease:
Diastolic blood pressure 		G 0.700 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878 2017
dbSNP: rs34712979
rs34712979
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0016529
Disease:
Forced expiratory volume function 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. 28166213 2017
dbSNP: rs34712979
rs34712979
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0042834
Disease:
Vital capacity 		A 0.700 GeneticVariation GWASCAT Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. 28166213 2017
dbSNP: rs34712979
rs34712979
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0016529
Disease:
Forced expiratory volume function 		A 0.700 GeneticVariation GWASCAT Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. 26423011 2015
dbSNP: rs6856422
rs6856422
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0016529
Disease:
Forced expiratory volume function 		G 0.700 GeneticVariation GWASCAT Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. 26635082 2015
dbSNP: rs7664805
rs7664805
Entrez Id: 255743
Gene Symbol: NPNT
NPNT
CUI: C0016529
Disease:
Forced expiratory volume function 		C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015