RS747349942 LAMA2

Health Risk Chr 6:129401254
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
LAMA2-related muscular dystrophy
Merosin deficient congenital muscular dystrophy
Inborn genetic diseases
Muscular dystrophy
limb-girdle
autosomal recessive 23
LAMA2-related muscular dystrophy
Merosin deficient congenital muscular dystrophy
Inborn genetic diseases
Muscular dystrophy
limb-girdle
autosomal recessive 23
Other Variants in LAMA2
rs121913569 rs121913571 rs2533535042 rs121913570 rs121913572 rs121913573 rs121913574 rs121913575 rs121913576 rs121913577
Ask Dr. Hemsworth about this variant