RS756317039 FN1
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Associated Conditions
Inborn genetic diseases
Spondylometaphyseal dysplasia - Sutcliffe type
Glomerulopathy with fibronectin deposits 2
Inborn genetic diseases
Spondylometaphyseal dysplasia - Sutcliffe type
Glomerulopathy with fibronectin deposits 2
Other Variants in FN1