RS140614229 LGI4

Health Risk Chr 19:35134620
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Associated Conditions
Arthrogryposis multiplex congenita 1
neurogenic
with myelin defect
Inborn genetic diseases
Arthrogryposis multiplex congenita 1
neurogenic
with myelin defect
Inborn genetic diseases
Other Variants in LGI4
rs1207534366 rs2513320717 rs2513330090 rs2065139570 rs2065190797 rs2065136111 rs1600470099 rs201728190 rs1201430967 rs779232987
Ask Dr. Hemsworth about this variant