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: 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: rs1064795155
rs1064795155
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0700635
Disease:
Strudwick syndrome
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1181638652
rs1181638652
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0700635
Disease:
Strudwick syndrome
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1373375768
rs1373375768
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs1553658926
rs1553658926
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0700635
Disease:
Strudwick syndrome
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1553659131
rs1553659131
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0700635
Disease:
Strudwick syndrome
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1553667072
rs1553667072
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0700635
Disease:
Strudwick syndrome
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1553669703
rs1553669703
Entrez Id: 2335;105373868
Gene Symbol: FN1;LOC105373868
FN1;LOC105373868
CUI: C0700635
Disease:
Strudwick syndrome
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1559604072
rs1559604072
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0700635
Disease:
Strudwick syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1559609410
rs1559609410
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0700635
Disease:
Strudwick syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs1559616744
rs1559616744
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0700635
Disease:
Strudwick syndrome
T 0.700 GeneticVariation CLINVAR
dbSNP: rs752106647
rs752106647
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C0006142
Disease:
Malignant neoplasm of breast
0.700 GeneticVariation UNIPROT
dbSNP: rs869025198
rs869025198
Entrez Id: 2335;112268430
Gene Symbol: FN1;LOC112268430
FN1;LOC112268430
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
G 0.700 CausalMutation CLINVAR
dbSNP: rs869025199
rs869025199
Entrez Id: 2335
Gene Symbol: FN1
FN1
CUI: C1866075
Disease:
GLOMERULOPATHY WITH FIBRONECTIN DEPOSITS 2 (disorder)
C 0.700 CausalMutation CLINVAR
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