RS141915593 CTSF

Health Risk Chr 11:66565008
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What This Variant Does
"CLNSIG=4
Associated Conditions
Neuronal ceroid lipofuscinosis 13
Inborn genetic diseases
Neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis 13
Inborn genetic diseases
Neuronal ceroid lipofuscinosis
Other Variants in CTSF
rs397514731 rs397514732 rs397514733 rs753084727 rs797045136 rs148611356 rs1555058286 rs141345438 rs573483617 rs143313688
Ask Dr. Hemsworth about this variant