RS587777669 HNRNPDL

Health Risk Chr 4:82426523
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal dominant limb-girdle muscular dystrophy type 1G
Autosomal dominant limb-girdle muscular dystrophy type 1G
HNRNPDL-related myopathy with protein aggregates and rimmed vacuoles
Autosomal dominant limb-girdle muscular dystrophy type 1G
Autosomal dominant limb-girdle muscular dystrophy type 1G
HNRNPDL-related myopathy with protein aggregates and rimmed vacuoles
Other Variants in HNRNPDL
rs763175161 rs373042980 rs1553901266 rs911762606 rs201774571 rs200595389 rs200123403 rs760683509 rs199543859 rs1447722708
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