RS80356682 LAMB3
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What This Variant Does
"rs80356682, also known as R635X, is a SNP in the laminin, beta 3 LAMB3 gene. This SNP is termed i501...
Associated Conditions
Junctional epidermolysis bullosa gravis of Herlitz
Junctional epidermolysis bullosa
non-Herlitz type
Amelogenesis imperfecta type 1A
LAMB3-related disorder
Junctional epidermolysis bullosa gravis of Herlitz
Junctional epidermolysis bullosa
non-Herlitz type
Amelogenesis imperfecta type 1A
LAMB3-related disorder
Other Variants in LAMB3