FN1, fibronectin 1, 2335

N. diseases: 724; N. variants: 33
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553658926
rs1553658926
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
C 0.800 GeneticVariation CLINVAR "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
dbSNP: rs1553658926
rs1553658926
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
0.800 GeneticVariation UNIPROT "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
dbSNP: rs1553659131
rs1553659131
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
C 0.800 GeneticVariation CLINVAR "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
dbSNP: rs1553659131
rs1553659131
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
0.800 GeneticVariation UNIPROT "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
dbSNP: rs1553667072
rs1553667072
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
G 0.800 GeneticVariation CLINVAR "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
dbSNP: rs1553667072
rs1553667072
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
0.800 GeneticVariation UNIPROT "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
dbSNP: rs1553669703
rs1553669703
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
A 0.800 GeneticVariation CLINVAR "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
dbSNP: rs1553669703
rs1553669703
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
0.800 GeneticVariation UNIPROT "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
dbSNP: rs137854486
rs137854486
Entrez Id: 2335;112268430
Gene Symbol: FN1;LOC112268430
FN1;LOC112268430
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FN1 cause glomerulopathy with fibronectin deposits. 18268355 2008
dbSNP: rs137854487
rs137854487
Entrez Id: 2335;112268430
Gene Symbol: FN1;LOC112268430
FN1;LOC112268430
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FN1 cause glomerulopathy with fibronectin deposits. 18268355 2008
dbSNP: rs137854488
rs137854488
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FN1 cause glomerulopathy with fibronectin deposits. 18268355 2008
dbSNP: rs137854486
rs137854486
Entrez Id: 2335;112268430
Gene Symbol: FN1;LOC112268430
FN1;LOC112268430
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
T 0.800 CausalMutation CLINVAR
dbSNP: rs137854487
rs137854487
Entrez Id: 2335;112268430
Gene Symbol: FN1;LOC112268430
FN1;LOC112268430
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
C 0.800 CausalMutation CLINVAR
dbSNP: rs137854487
rs137854487
Entrez Id: 2335;112268430
Gene Symbol: FN1;LOC112268430
FN1;LOC112268430
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
G 0.800 CausalMutation CLINVAR
dbSNP: rs137854488
rs137854488
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
C 0.800 CausalMutation CLINVAR
dbSNP: rs1553659131
rs1553659131
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
C 0.800 CausalMutation CLINVAR
dbSNP: rs1553667072
rs1553667072
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
G 0.800 CausalMutation CLINVAR
dbSNP: rs1553669703
rs1553669703
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0432221
Disease:
Spondylometaphyseal dysplasia, 'corner fracture' type
A 0.800 CausalMutation CLINVAR
dbSNP: rs1250248
rs1250248
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0042834
Disease:
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1250258
rs1250258
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0205682
Disease:
Waist-Hip Ratio
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1250259
rs1250259
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0871470
Disease:
Systolic Pressure
T 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs1250259
rs1250259
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0428883
Disease:
Diastolic blood pressure
T 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs1250259
rs1250259
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0871470
Disease:
Systolic Pressure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1250259
rs1250259
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0205682
Disease:
Waist-Hip Ratio
A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs1250259
rs1250259
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
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