RS140213840 MMP20
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Amelogenesis imperfecta hypomaturation type 2A2
MMP20-related disorder
Inborn genetic diseases
Gastric cancer
Amelogenesis imperfecta hypomaturation type 2A2
MMP20-related disorder
Inborn genetic diseases
Gastric cancer
Other Variants in MMP20