RS200123403 HNRNPDL

Health Risk Chr 4:82426558
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Associated Conditions
Autosomal dominant limb-girdle muscular dystrophy type 1G
Autosomal dominant limb-girdle muscular dystrophy type 1G
Other Variants in HNRNPDL
rs587777669 rs763175161 rs373042980 rs1553901266 rs911762606 rs201774571 rs200595389 rs760683509 rs199543859 rs1447722708
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