RS587780362 ITGA7
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital muscular dystrophy due to integrin alpha-7 deficiency
Congenital muscular dystrophy due to integrin alpha-7 deficiency
Congenital muscular dystrophy due to integrin alpha-7 deficiency
Congenital muscular dystrophy due to integrin alpha-7 deficiency
Other Variants in ITGA7