RS1386551513 CTSC

Health Risk Chr 11:88294481
Upload your DNA to see your genotype for this variant.
Associated Conditions
Periodontitis
aggressive 1
Papillon-Lefèvre syndrome
Haim-Munk syndrome
Inborn genetic diseases
Periodontitis
aggressive 1
Papillon-Lefèvre syndrome
Haim-Munk syndrome
Inborn genetic diseases
Other Variants in CTSC
rs104894206 rs587776654 rs104894207 rs104894209 rs587776655 rs104894208 rs104894210 rs104894214 rs104894215 rs28937571
Ask Dr. Hemsworth about this variant