RS200402328 ITGA7

Health Risk Chr 12:55694442
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital muscular dystrophy due to integrin alpha-7 deficiency
ITGA7-related disorder
Congenital muscular dystrophy due to integrin alpha-7 deficiency
ITGA7-related disorder
Other Variants in ITGA7
rs1565627745 rs774985604 rs1565629479 rs149081471 rs144983062 rs587780362 rs142311782 rs761067098 rs149028067 rs148641361
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