RS9492297 LAMA2

Health Risk Chr 6:129291612 snv splice acceptor variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
LAMA2-related muscular dystrophy
LAMA2-related muscular dystrophy
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