RS779232987 LGI4

Health Risk Chr 19:35126853
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What This Variant Does
"CLNSIG=5
Associated Conditions
Arthrogryposis multiplex congenita 1
neurogenic
with myelin defect
Arthrogryposis multiplex congenita 1
neurogenic
with myelin defect
Other Variants in LGI4
rs1201430967 rs2513320717 rs2513330090 rs140614229 rs2065139570 rs2065190797 rs2065136111 rs1600470099 rs201728190 rs775997446
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