RS2482767087 LAMA2

Health Risk Chr 6:129190226
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Associated Conditions
Inborn genetic diseases
Merosin deficient congenital muscular dystrophy
Inborn genetic diseases
Merosin deficient congenital muscular dystrophy
Other Variants in LAMA2
rs121913569 rs121913571 rs2533535042 rs121913570 rs121913572 rs121913573 rs121913574 rs121913575 rs121913576 rs121913577
Ask Dr. Hemsworth about this variant