RS139739075 LAMA2

Health Risk Chr 6:129316122 snv missense variant
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Associated Conditions
LAMA2-related muscular dystrophy
Merosin deficient congenital muscular dystrophy
Congenital muscular dystrophy due to partial LAMA2 deficiency
Muscular dystrophy
limb-girdle
autosomal recessive 23
LAMA2-related muscular dystrophy
Merosin deficient congenital muscular dystrophy
Congenital muscular dystrophy due to partial LAMA2 deficiency
Muscular dystrophy
limb-girdle
autosomal recessive 23
Population Frequencies
gnomAD ALL
100%
Other Variants in LAMA2
rs121913569 rs121913571 rs2533535042 rs121913570 rs121913572 rs121913573 rs121913574 rs121913575 rs121913576 rs121913577
Ask Dr. Hemsworth about this variant