RS1021613206 CTSD

Health Risk Chr 11:1763797
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Associated Conditions
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Neuronal ceroid lipofuscinosis
Inborn genetic diseases
Other Variants in CTSD
rs121912789 rs121912790 rs786205105 rs140238987 rs374010531 rs113936232 rs587780914 rs147641822 rs587780917 rs146073498
Ask Dr. Hemsworth about this variant