RS193922922 KIF22
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spondyloepimetaphyseal dysplasia with multiple dislocations
Inborn genetic diseases
See cases
Spondyloepimetaphyseal dysplasia with multiple dislocations
Spondyloepimetaphyseal dysplasia with multiple dislocations
Inborn genetic diseases
See cases
Spondyloepimetaphyseal dysplasia with multiple dislocations
Other Variants in KIF22