RS587777814 FKTN

Health Risk Chr 9:105635239
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2M
Autosomal recessive limb-girdle muscular dystrophy type 2M
Other Variants in FKTN
rs119463990 rs587777813 rs398123555 rs119463996 rs587777748 rs119463991 rs119463992 rs119463993 rs119463994 rs2539985441
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