RS765305996 ECEL1

Health Risk Chr 2:232486160
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Associated Conditions
Inborn genetic diseases
Arthrogryposis multiplex congenita
Distal arthrogryposis type 5D
Inborn genetic diseases
Arthrogryposis multiplex congenita
Distal arthrogryposis type 5D
Other Variants in ECEL1
rs587776917 rs587776918 rs587776919 rs587776920 rs587777129 rs587777130 rs587777131 rs606231471 rs532757890 rs368488157
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