rs1553658926, FN1

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Spondylometaphyseal dysplasia, 'corner fracture' type
0.800 GeneticVariation CLINVAR "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
Spondylometaphyseal dysplasia, 'corner fracture' type
0.800 GeneticVariation UNIPROT "Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with ""Corner Fractures""." 29100092 2017
Strudwick syndrome
CUI: C0700635
Disease: Strudwick syndrome
0.700 GeneticVariation CLINVAR