RS115650537 LAMA2

Health Risk Chr 6:129502695 snv missense variant
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What This Variant Does
"CLNSIG=5
Associated Conditions
LAMA2-related muscular dystrophy
Congenital muscular dystrophy due to partial LAMA2 deficiency
LAMA2-related disorder
LAMA2-related muscular dystrophy
Congenital muscular dystrophy due to partial LAMA2 deficiency
LAMA2-related disorder
Population Frequencies
gnomAD ALL
0%
1kG AFR
99.6%
1kG ALL
0.1%
1kG AMR
99.9%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in LAMA2
rs121913569 rs121913571 rs2533535042 rs121913570 rs121913572 rs121913573 rs121913574 rs121913575 rs121913576 rs121913577
Ask Dr. Hemsworth about this variant