RS193922921 KIF22

Health Risk Chr 16:29798641
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spondyloepimetaphyseal dysplasia with multiple dislocations
Inborn genetic diseases
Spondyloepimetaphyseal dysplasia with multiple dislocations
Inborn genetic diseases
Other Variants in KIF22
rs201726114 rs201572301 rs750463562 rs372337472 rs767054899 rs370133905 rs776568168 rs1396521687 rs751762149 rs1267445233
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