Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4894535
rs4894535
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0524957
Disease:
Corneal Topography 		T 0.800 GeneticVariation GWASCAT Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. 23291589 2013
dbSNP: rs4894535
rs4894535
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0524957
Disease:
Corneal Topography 		T 0.800 GeneticVariation GWASDB Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. 23291589 2013
dbSNP: rs9647379
rs9647379
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0018810
Disease:
heart rate 		C 0.800 GeneticVariation GWASCAT Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. 23583979 2013
dbSNP: rs9647379
rs9647379
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0018810
Disease:
heart rate 		C 0.800 GeneticVariation GWASDB Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. 23583979 2013
dbSNP: rs11718418
rs11718418
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs12492846
rs12492846
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0040420
Disease:
Tonometry 		C 0.700 GeneticVariation GWASCAT Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. 29785010 2018
dbSNP: rs12492846
rs12492846
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0040420
Disease:
Tonometry 		0.700 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594 2018
dbSNP: rs12493901
rs12493901
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0037369
Disease:
Smoking 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
dbSNP: rs12493901
rs12493901
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C4049938
Disease:
Physical Activity Measurement 		G 0.700 GeneticVariation GWASCAT Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. 28448500 2017
dbSNP: rs12493901
rs12493901
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C1519383
Disease:
Smoking Behaviors 		A 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. 28443625 2017
dbSNP: rs12897
rs12897
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C1956346
Disease:
Coronary Artery Disease 		A 0.700 GeneticVariation GWASCAT Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. 29212778 2018
dbSNP: rs16856859
rs16856859
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs16856859
rs16856859
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs16856911
rs16856911
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0040420
Disease:
Tonometry 		0.700 GeneticVariation GWASCAT Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. 30054594 2018
dbSNP: rs35461662
rs35461662
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0427460
Disease:
Red cell distribution width determination 		A 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
dbSNP: rs35461662
rs35461662
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		A 0.700 GeneticVariation GWASCAT Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. 28957414 2017
dbSNP: rs397778518
rs397778518
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0206161
Disease:
Reticulocyte count (procedure) 		CT 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs4243400
rs4243400
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0005890
Disease:
Body Height 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. 25429064 2015
dbSNP: rs4243400
rs4243400
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs4380442
rs4380442
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0040420
Disease:
Tonometry 		G 0.700 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998 2018
dbSNP: rs4535251
rs4535251
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0005890
Disease:
Body Height 		T 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
dbSNP: rs4535251
rs4535251
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0489786
Disease:
Height 		T 0.700 GeneticVariation GWASDB Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. 23563607 2013
dbSNP: rs4894539
rs4894539
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs4894797
rs4894797
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs4894797
rs4894797
Entrez Id: 64778
Gene Symbol: FNDC3B
FNDC3B
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019