RS750157767 CTSC

Health Risk Chr 11:88337657
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Associated Conditions
Inborn genetic diseases
Haim-Munk syndrome
Papillon-Lefèvre syndrome
Periodontitis
aggressive 1
Inborn genetic diseases
Haim-Munk syndrome
Papillon-Lefèvre syndrome
Periodontitis
aggressive 1
Other Variants in CTSC
rs104894206 rs587776654 rs104894207 rs104894209 rs587776655 rs104894208 rs104894210 rs104894214 rs104894215 rs28937571
Ask Dr. Hemsworth about this variant