rs1553658926
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
C |
0.800 |
GeneticVariation |
CLINVAR |
"Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""."
|
29100092 |
2017 |
rs1553658926
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
|
0.800 |
GeneticVariation |
UNIPROT |
"Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""."
|
29100092 |
2017 |
rs1553659131
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
C |
0.800 |
GeneticVariation |
CLINVAR |
"Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""."
|
29100092 |
2017 |
rs1553659131
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
|
0.800 |
GeneticVariation |
UNIPROT |
"Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""."
|
29100092 |
2017 |
rs1553667072
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
G |
0.800 |
GeneticVariation |
CLINVAR |
"Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""."
|
29100092 |
2017 |
rs1553667072
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
|
0.800 |
GeneticVariation |
UNIPROT |
"Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""."
|
29100092 |
2017 |
rs1553669703
|
FN1;LOC105373868
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
A |
0.800 |
GeneticVariation |
CLINVAR |
"Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""."
|
29100092 |
2017 |
rs1553669703
|
FN1;LOC105373868
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
|
0.800 |
GeneticVariation |
UNIPROT |
"Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""."
|
29100092 |
2017 |
rs137854486
|
FN1;LOC112268430
|
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
|
18268355 |
2008 |
rs137854487
|
FN1;LOC112268430
|
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
|
18268355 |
2008 |
rs137854488
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
|
|
0.800 |
GeneticVariation |
UNIPROT |
Mutations in FN1 cause glomerulopathy with fibronectin deposits.
|
18268355 |
2008 |
rs137854486
|
FN1;LOC112268430
|
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs137854487
|
FN1;LOC112268430
|
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs137854487
|
FN1;LOC112268430
|
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs137854488
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1553659131
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1553667072
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
G |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1553669703
|
FN1;LOC105373868
|
Spondylometaphyseal dysplasia, 'corner fracture' type
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1250248
|
Entrez Id: |
2335 |
Gene Symbol: |
FN1 |
FN1
|
Vital capacity
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs1250258
|
FN1;LOC105373868
|
Waist-Hip Ratio
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs1250259
|
FN1;LOC105373868
|
Systolic Pressure
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
|
30578418 |
2019 |
rs1250259
|
FN1;LOC105373868
|
Diastolic blood pressure
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.
|
30578418 |
2019 |
rs1250259
|
FN1;LOC105373868
|
Systolic Pressure
|
|
0.700 |
GeneticVariation |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
rs1250259
|
FN1;LOC105373868
|
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 |
rs1250259
|
FN1;LOC105373868
|
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 |