RS786205083 DYSF

Health Risk Chr 2:71590178
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2B
Autosomal recessive limb-girdle muscular dystrophy type 2B
Other Variants in DYSF
rs121908953 rs786205081 rs121908955 rs786200896 rs786205082 rs121908956 rs745891180 rs121908957 rs28937581 rs121908958
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