RS61751462 MMP20

Health Risk Chr 11:102625217
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Associated Conditions
Amelogenesis imperfecta hypomaturation type 2A2
Inborn genetic diseases
Amelogenesis imperfecta hypomaturation type 2A2
Inborn genetic diseases
Other Variants in MMP20
rs61753770 rs781178683 rs759614533 rs761478767 rs1859555583 rs199788797 rs1565397250 rs916966344 rs17098831 rs140213840
Ask Dr. Hemsworth about this variant