RS587780291 CAPN3

Health Risk Chr 15:42384544
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What This Variant Does
"CLNSIG=4
Associated Conditions
Autosomal recessive limb-girdle muscular dystrophy type 2A
Inborn genetic diseases
Autosomal recessive limb-girdle muscular dystrophy type 2A
Inborn genetic diseases
Other Variants in CAPN3
rs80338802 rs121434544 rs121434545 rs121434546 rs121434547 rs1555423217 rs267606703 rs80338803 rs80338800 rs121434548
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